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XB-GENEPAGE-478293
rab28 RAB28, member RAS oncogene family
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, Foveal atrophy, Foveal hyperpigmentation, High myopia, Nyctalopia, Photophobia, Visual impairment |
Mouse (12 sources): abnormal PQ interval, abnormal PR interval, abnormal heart weight, abnormal retina cone cell morphology, abnormal retina cone cell outer segment morphology, abnormal retina outer nuclear layer thickness, decreased a-wave amplitude, decreased b-wave amplitude, decreased heart weight, increased thigmotaxis, [+] |
View all ortholog results at Monarch |