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XB-GENEPAGE-484312
slc9a1 solute carrier family 9 member 1
Monarch Ortholog Phenotypes
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Human (11 sources): Action tremor, Ataxia, Cerebellar atrophy, Dysarthria, Dysdiadochokinesis, Dysmetria, Gait ataxia, Limb ataxia, Motor delay, Nystagmus, [+] |
Mouse (33 sources): Purkinje cell degeneration, abnormal PR interval, abnormal Purkinje cell morphology, abnormal axon morphology, abnormal cerebellar molecular layer, abnormal cerebellum deep nucleus morphology, abnormal cerebellum dentate nucleus morphology, abnormal epidermis stratum corneum morphology, abnormal fertility/fecundity, abnormal locomotor coordination, [+] |
View all ortholog results at Monarch |