Symbol
Name
ID

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

Phenotype annotations related to vision/eye

Darker colors indicate more annotations

Human Phenotypes

Macular edema

Cataract

Posterior subcapsular cataract

Nuclear cataract

Cystoid macular degeneration

Pigmentary retinopathy

Rod-cone dystrophy

Retinoschisis

Vitreoretinopathy

Undetectable light- and dark-adapted electroretinogram

Undetectable electroretinogram

Tritanomaly

Red-green dyschromatopsia

Hemeralopia

Nyctalopia

Photophobia

Reduced visual acuity

Constriction of peripheral visual field

Disease(s) Associated with NR2E3

enhanced S-cone syndrome

retinitis pigmentosa 37

Mouse Phenotypes		increased retina apoptosis	abnormal retina photoreceptor morphology	short photoreceptor outer segment	abnormal retina cone cell morphology	abnormal retina outer nuclear layer morphology	disorganized retina outer nuclear layer	retina outer nuclear layer degeneration	retina degeneration	abnormal cone electrophysiology	abnormal rod electrophysiology
Availability	Mouse Genotype	increased retina apoptosis	abnormal retina photoreceptor morphology	short photoreceptor outer segment	abnormal retina cone cell morphology	abnormal retina outer nuclear layer morphology	disorganized retina outer nuclear layer	retina outer nuclear layer degeneration	retina degeneration	abnormal cone electrophysiology	abnormal rod electrophysiology
	Nr2e3^rd7/Nr2e3^rd7
	Nr2e3^tm1Dgen/Nr2e3^tm1Dgen

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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