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XB-GENEPAGE-944929
poc1b POC1 centriolar protein B
Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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Human (10 sources): Abnormality of retinal pigmentation, Central scotoma, Color vision defect, Cone/cone-rod dystrophy, Constriction of peripheral visual field, Nyctalopia, Nystagmus, Photophobia, Reduced visual acuity, Visual impairment |
View all ortholog results at Monarch |