Nr1d2 Phenotype Annotations

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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

10 phenotypes from 3 alleles in 4 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Nr1d2^tm1.1Pbrc/Nr1d2^tm1.1Pbrc involves: C57BL/6J	impaired behavioral response to xenobiotic	J:225389
Nr1d2^tm1.1Pbrc/Nr1d2^tm1.1Pbrc involves: C57BL/6J	increased anxiety-related response	J:225389
Nr1d2^tm1.2Rev/Nr1d2^tm1.2Rev involves: BALB/cJ * C57BL/6J	no abnormal phenotype detected	J:183855
Nr1d2^tm1Dgen/Nr1d2⁺ B6;129P2-Nr1d2^tm1Dgen/H	neonatal lethality, incomplete penetrance	J:232480
Nr1d2^tm1Dgen/Nr1d2^tm1Dgen B6;129P2-Nr1d2^tm1Dgen/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
Nr1d2^tm1Dgen/Nr1d2^tm1Dgen 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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