reep6 Phenotypes

Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Phenotypes

XB-GENEPAGE-974920

Gene Symbol: reep6 Gene Name: receptor accessory protein 6

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (34 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 edema, Glaucoma, Hyperinsulinemia, Hyperreflexia, Hypogonadism, Hypoplasia of penis, Intellectual disability, Keratoconus, Nyctalopia, Nystagmus, Obesity, Ophthalmoplegia, Optic atrophy, Photophobia, Posterior subcapsular cataract, Progressive night blindness, Reduced visual acuity, Retinal atrophy, Rod-cone dystrophy, Sensorineural hearing impairment, Type II diabetes mellitus, Visual impairment, Wide nasal bridge [+]
Mouse (16 sources): abnormal electroretinogram waveform feature, abnormal photoreceptor inner segment morphology, abnormal photoreceptor outer segment disc membrane morphology, abnormal photoreceptor outer segment morphology, abnormal retina rod cell morphology, abnormal rod electrophysiology, asthenozoospermia, decreased a-wave amplitude, decreased b-wave amplitude, impaired acrosome reaction, increased endoplasmic reticulum stress, photoreceptor inner segment degeneration, photoreceptor outer segment degeneration, retina outer nuclear layer degeneration, retina photoreceptor degeneration, thin retina outer nuclear layer [+]
View all ortholog results at Monarch