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XB-GENEPAGE-1005706
oat.2 ornithine aminotransferase, gene 2
Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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Human (21 sources): Abnormal hair morphology, Abnormal macular morphology, Abnormality of metabolism/homeostasis, Aminoaciduria, Blindness, Cataract, Chorioretinal atrophy, Chorioretinal degeneration, Chorioretinal hyperpigmentation, Constriction of peripheral visual field, [+] |
Mouse (19 sources): abnormal eye electrophysiology, abnormal hair follicle morphology, abnormal retina pigment epithelium morphology, absent photoreceptor outer segment, decreased body size, decreased circulating alkaline phosphatase level, decreased circulating amylase level, decreased circulating thyroxine level, decreased retina photoreceptor cell number, disorganized photoreceptor inner segment, [+] |
View all ortholog results at Monarch |