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XB-GENEPAGE-1012637
grk1 G protein-coupled receptor kinase 1
Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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Human (1 source): Congenital stationary night blindness |
Mouse (8 sources): abnormal electroretinogram waveform feature, abnormal retina apoptosis, abnormal retina rod cell morphology, abnormal retina rod cell outer segment morphology, abnormal rod electrophysiology, decreased total retina thickness, retina photoreceptor degeneration, retina spots |
View all ortholog results at Monarch |