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XB-GENEPAGE-960508
rp1l1 retinitis pigmentosa 1 like 1
Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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Human (3 sources): Abnormal multifocal electroretinogram, Macular dystrophy, Slow decrease in visual acuity |
Mouse (7 sources): abnormal cone electrophysiology, abnormal photoreceptor outer segment morphology, abnormal rod electrophysiology, decreased retina photoreceptor cell number, retina rod cell degeneration, short photoreceptor outer segment, thin retina outer nuclear layer |
View all ortholog results at Monarch |