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XB-GENEPAGE-1008689
sptbn2 spectrin, beta, non-erythrocytic 2
Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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Human (34 sources): Abnormality of eye movement, Cerebellar atrophy, Cognitive impairment, Delayed speech and language development, Diplopia, Dysarthria, Dysdiadochokinesis, Dysmetria, Dysmetric saccades, Facial myokymia, [+] |
Mouse (12 sources): Purkinje cell degeneration, abnormal Purkinje cell dendrite morphology, abnormal Purkinje cell morphology, abnormal cerebellar molecular layer, abnormal circulating total protein level, behavior/neurological phenotype, clonic seizures, decreased hemoglobin content, impaired balance, increased excitatory postsynaptic current amplitude, [+] |
View all ortholog results at Monarch |