Nr2e3 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Nr2e3
nuclear receptor subfamily 2, group E, member 3
MGI:1346317

10 phenotypes from 2 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Nr2e3^rd7/Nr2e3^rd7 B6.Cg-Nr2e3^rd7/J	abnormal retina cone cell morphology	J:107820
	abnormal retina outer nuclear layer morphology	J:107820
	abnormal retina photoreceptor morphology	J:107820
	disorganized retina outer nuclear layer	J:148636
	increased retina apoptosis	J:148636
	retina outer nuclear layer degeneration	J:148636
	short photoreceptor outer segment	J:148636
Nr2e3^rd7/Nr2e3^rd7 Not Specified	abnormal cone electrophysiology	J:62171
	abnormal rod electrophysiology	J:62171
	retina degeneration	J:62171
Nr2e3^tm1Dgen/Nr2e3^tm1Dgen involves: 129P2/OlaHsd * C57BL/6J	abnormal retina outer nuclear layer morphology	J:138242

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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