nr2e3 Phenotypes

Phenotypes

XB-GENEPAGE-485800

Gene Symbol: nr2e3 Gene Name: nuclear receptor subfamily 2 group E member 3

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (41 sources): Abnormal electroretinogram, Abnormal retinal vascular morphology, Abnormal testis morphology, Abnormality of fundus pigmentation, Abnormality of retinal pigmentation, Anteverted nares, Atypical scarring of skin, Blindness, Cataract, Conductive hearing impairment, Constriction of peripheral visual field, Cystoid macular degeneration, Edema, Glaucoma, Hemeralopia, Hyperinsulinemia, Hyperreflexia, Hypogonadism, Hypoplasia of penis, Intellectual disability, Keratoconus, Macular edema, Nyctalopia, Nystagmus, Obesity, Ophthalmoplegia, Optic atrophy, Photophobia, Pigmentary retinopathy, Progressive night blindness, Red-green dyschromatopsia, Retinoschisis, Rod-cone dystrophy, Sensorineural hearing impairment, Tritanomaly, Type II diabetes mellitus, Undetectable electroretinogram, Undetectable light- and dark-adapted electroretinogram, Visual impairment, Vitreoretinopathy, Wide nasal bridge [+]
Mouse (9 sources): abnormal cone electrophysiology, abnormal retina cone cell morphology, abnormal retina outer nuclear layer morphology, abnormal retina photoreceptor morphology, abnormal rod electrophysiology, disorganized retina outer nuclear layer, increased retina apoptosis, retina outer nuclear layer degeneration, short photoreceptor outer segment
View all ortholog results at Monarch