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XB-GENEPAGE-1010370
slc7a14 solute carrier family 7 member 14
Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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Human (32 sources): Abnormal electroretinogram, Abnormal retinal vascular morphology, Abnormal testis morphology, Abnormality of fundus pigmentation, Abnormality of retinal pigmentation, Anteverted nares, Atypical scarring of skin, Blindness, Cataract, Conductive hearing impairment, [+] |
Mouse (5 sources): abnormal eye electrophysiology, abnormal rod electrophysiology, decreased total retina thickness, increased circulating creatinine level, thin retina outer nuclear layer |
View all ortholog results at Monarch |