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XB-GENEPAGE-957296
ush2a Usher syndrome 2A (autosomal recessive, mild)
Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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| Human (66 sources): Abnormal cardiovascular system physiology, Abnormal dental enamel morphology, Abnormal electroretinogram, Abnormal retinal vascular morphology, Abnormal testis morphology, Abnormality of dental color, Abnormality of fundus pigmentation, Abnormality of retinal pigmentation, Abnormality of the inner ear, Anteverted nares, [+] |
| Mouse (9 sources): abnormal distortion product otoacoustic emission, abnormal eye electrophysiology, abnormal retina photoreceptor layer morphology, abnormal retina photoreceptor morphology, decreased cochlear outer hair cell number, retina cone cell degeneration, retina photoreceptor degeneration, short photoreceptor inner segment, short photoreceptor outer segment |
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View all ortholog results at Monarch |