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XB-GENEPAGE-6036031
atp8a2 ATPase, aminophospholipid transporter, class I, type 8A, member 2
Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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Human (15 sources): Abnormality of movement, Abnormality of the orbital region, Abnormality of vision, Ataxia, Cataract, Cerebral palsy, Cleft palate, Gait disturbance, Hyperreflexia, Hypotonia, [+] |
Mouse (37 sources): abnormal cone electrophysiology, abnormal enterocyte morphology, abnormal enzyme/coenzyme level, abnormal retina cone cell outer segment morphology, abnormal retina pigment epithelium morphology, abnormal rod electrophysiology, abnormal spinal cord white matter morphology, abnormal startle reflex, abnormal voluntary movement, axonal dystrophy, [+] |
View all ortholog results at Monarch |