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XB-GENEPAGE-991429
slc24a1 solute carrier family 24 member 1
Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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Human (11 sources): Abnormal fundus morphology, Abnormal retinal morphology, Abnormality of macular pigmentation, Blindness, Congenital stationary night blindness, High myopia, Nyctalopia, Nystagmus, Optic disc hypoplasia, Reduced visual acuity, [+] |
Mouse (6 sources): abnormal a-wave shape, abnormal photoreceptor outer segment morphology, abnormal retina cone cell outer segment morphology, abnormal rod electrophysiology, retina rod cell degeneration, thin retina outer nuclear layer |
View all ortholog results at Monarch |