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XB-GENEPAGE-5848873
rs1 retinoschisin 1
Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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Human (18 sources): Abnormal electroretinogram, Abnormality of eye movement, Abnormality of the orbital region, Abnormality of vision, Cataract, Electronegative electroretinogram, Glaucoma, Hypermetropia, Macular atrophy, Mizuo phenomenon, [+] |
Mouse (37 sources): abnormal Muller cell morphology, abnormal amacrine cell morphology, abnormal astrocyte morphology, abnormal cone electrophysiology, abnormal electroretinogram waveform feature, abnormal eye electrophysiology, abnormal innervation, abnormal neuron physiology, abnormal photoreceptor inner segment morphology, abnormal photoreceptor outer segment morphology, [+] |
View all ortholog results at Monarch |