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XB-GENEPAGE-1007973
rpgrip1 RPGR interacting protein 1
Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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Human (28 sources): Abnormal electroretinogram, Abnormality of neuronal migration, Abnormality of retinal pigmentation, Abnormality of the optic disc, Aplasia/Hypoplasia of the cerebellar vermis, Attenuation of retinal blood vessels, Cataract, Color vision defect, Cone/cone-rod dystrophy, Encephalocele, [+] |
Mouse (13 sources): abnormal cone electrophysiology, abnormal electroretinogram waveform feature, abnormal photoreceptor outer segment morphology, abnormal rod electrophysiology, absent photoreceptor outer segment, decreased a-wave amplitude, decreased b-wave amplitude, disorganized photoreceptor outer segment, retina photoreceptor degeneration, retina spots, [+] |
View all ortholog results at Monarch |