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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Nr1d2
nuclear receptor subfamily 1, group D, member 2
MGI:2449205
11 phenotypes from 4 alleles in 5 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Nr1d2em1(IMPC)Mbp/Nr1d2em1(IMPC)Mbp
C57BL/6N-Nr1d2em1(IMPC)Mbp/Ucd
increased circulating alanine transaminase level J:211773
Nr1d2tm1.1Pbrc/Nr1d2tm1.1Pbrc
involves: C57BL/6J
impaired behavioral response to xenobiotic J:225389
increased anxiety-related response J:225389
Nr1d2tm1.2Rev/Nr1d2tm1.2Rev
involves: BALB/cJ * C57BL/6J
no abnormal phenotype detected J:183855
Nr1d2tm1Dgen/Nr1d2+
B6;129P2-Nr1d2tm1Dgen/H
neonatal lethality, incomplete penetrance J:232480
Nr1d2tm1Dgen/Nr1d2tm1Dgen
B6;129P2-Nr1d2tm1Dgen/H
abnormal heart morphology J:232480
atrioventricular septal defect J:232480
common atrioventricular valve J:232480
inlet ventricular septal defect J:232480
neonatal lethality, incomplete penetrance J:232480
ostium primum atrial septal defect J:232480
Nr1d2tm1Dgen/Nr1d2tm1Dgen
involves: 129P2/OlaHsd * C57BL/6J
no abnormal phenotype detected J:82809
preweaning lethality, incomplete penetrance J:82809

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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last database update
04/30/2024
MGI 6.23
The Jackson Laboratory