cerebellar ataxia; Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A cerebellar disease characterized by ataxia originating in the cerebellum. (Human Disease Ontology, DOID_0050753)
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10 genes associated with the disease cerebellar ataxia; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
ATXN1 ataxin 1
ATXN10 ataxin 10
ATXN2 ataxin 2
ATXN3 ataxin 3
ATXN7 ataxin 7
ATXN8 ataxin 8
CACNA1A calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
FXN frataxin
PPP2R2B protein phosphatase 2, regulatory subunit B, beta
TBP TATA box binding protein