rp1 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

Gene Literature (2)

Nucleotides (24)

Interactants (15)

XB-GENEPAGE-6032684

Gene Symbol: rp1 Gene Name: RP1, axonemal microtubule associated

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (33 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, Bone spicule pigmentation of the retina, Cataract, Conductive hearing impairment, Constriction of peripheral visual field, Glaucoma, Hyperinsulinemia, Hyperreflexia, Hypogonadism, Hypoplasia of penis, Intellectual disability, Keratoconus, Myopia, Nyctalopia, Nystagmus, Obesity, Ophthalmoplegia, Optic atrophy, Photophobia, Progressive night blindness, Rod-cone dystrophy, Sensorineural hearing impairment, Type II diabetes mellitus, Undetectable light- and dark-adapted electroretinogram, Visual impairment, Wide nasal bridge [+]
Mouse (19 sources): abnormal cone electrophysiology, abnormal eye electrophysiology, abnormal photoreceptor outer segment morphology, abnormal retina neuronal layer morphology, abnormal retina photoreceptor morphology, abnormal retina vasculature morphology, abnormal rod electrophysiology, decreased a-wave amplitude, decreased b-wave amplitude, decreased retina photoreceptor cell number, disorganized photoreceptor inner segment, disorganized photoreceptor outer segment, retina cone cell degeneration, retina photoreceptor degeneration, retina rod cell degeneration, short photoreceptor inner segment, short photoreceptor outer segment, thin retina outer nuclear layer, vision/eye phenotype [+]
View all ortholog results at Monarch