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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Jarid2
jumonji and AT-rich interaction domain containing 2
MGI:104813
56 phenotypes from 5 alleles in 8 genetic backgrounds
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Allelic Composition
Genetic Background		 Annotated Term Reference
Jarid2Gt(pGT1.8geo)6Pgr/Jarid2Gt(pGT1.8geo)6Pgr
either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ) 		abnormal nervous system development J:47982
edema J:47982
prenatal lethality J:47982
Jarid2Gt(ROSA)1Gel/Jarid2Gt(ROSA)1Gel
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 		abnormal coronary vessel morphology J:63359
abnormal fetal cardiomyocyte proliferation J:100923
abnormal interventricular groove morphology J:63359
abnormal interventricular septum morphology J:63359
abnormal myocardium compact layer morphology J:63359
abnormal myocardium layer morphology J:63359
abnormal sternum morphology J:63359
abnormal thoracic cage morphology J:63359
decreased embryo size J:63359
dilated heart right atrium J:63359
double outlet right ventricle J:63359
edema J:63359
perinatal lethality, complete penetrance J:63359
respiratory failure J:63359
thin myocardium J:63359
trabecula carnea hypoplasia J:63359
ventricular septal defect J:63359
Jarid2jumonji/Jarid2jumonji
C3.129P2-Jarid2jumonji 		abnormal heart development J:57069
abnormal heart left ventricle morphology J:57069
abnormal myocardial fiber morphology J:57069
abnormal myocardial trabeculae morphology J:57069
abnormal neural plate morphology J:57069
abnormal neural tube morphology J:57069
decreased embryo size J:57069
delayed neural tube closure J:57069
embryonic lethality during organogenesis, complete penetrance J:57069
incomplete rostral neuropore closure J:57069
Jarid2jumonji/Jarid2jumonji
C.129P2-Jarid2jumonji 		abnormal definitive hematopoiesis J:51843
abnormal erythropoiesis J:51843
abnormal liver morphology J:42772
abnormal liver physiology J:85152
abnormal megakaryocyte progenitor cell morphology J:68443
abnormal splenic cell ratio J:42772
abnormal thymus cell ratio J:42772
anemia J:51843
decreased fetal derived definitive erythrocyte cell number J:51843
decreased hepatocyte number J:85152
dilated liver sinusoidal space J:42772
distended pericardium J:42772
edema J:42772
fetal growth retardation J:42772
hemorrhage J:42772
hepatic necrosis J:42772
lethality throughout fetal growth and development, complete penetrance J:42772
liver hypoplasia J:42772
normal nervous system phenotype J:42772
small liver J:85152
spleen hypoplasia J:42772
thymus hypoplasia J:42772
Jarid2jumonji/Jarid2jumonji
either: B6.129P2-Jarid2jumonji or D2.129P2-Jarid2jumonji 		edema J:42772
lethality throughout fetal growth and development, complete penetrance J:42772
liver hypoplasia J:42772
normal nervous system phenotype J:42772
spleen hypoplasia J:42772
thymus hypoplasia J:42772
Jarid2jumonji/Jarid2jumonji
involves: 129P2/OlaHsd * BALB/cA 		abnormal nervous system development J:25641
abnormal neural fold formation J:25641
abnormal neural tube closure J:25641
delayed neural tube closure J:25641
edema J:25641
embryonic lethality during organogenesis, incomplete penetrance J:25641
lethality throughout fetal growth and development, incomplete penetrance J:25641
Jarid2tm1a(KOMP)Wtsi/Jarid2+
Not Specified 		increased body length J:165965
increased circulating creatinine level J:175295
Jarid2tm1Yskl/Jarid2tm1Yskl
Tg(Myh6-cre)2182Mds/0
involves: 129S1/Sv * 129X1/SvJ * FVB/N 		no abnormal phenotype detected J:114450
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory