spinocerebellar ataxia Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A spinocerebellar degeneration that is characterized by degeneration of the cerebellum leading to loss of muscle coordination. (Human Disease Ontology, DOID_1441)
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16 genes associated with the disease spinocerebellar ataxia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
ATN1 atrophin 1
ATXN1 ataxin 1
ATXN10 ataxin 10
ATXN2 ataxin 2
ATXN3 ataxin 3
ATXN7 ataxin 7
ATXN8OS ATXN8 opposite strand (non-protein coding)
CACNA1A calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
FGF14 fibroblast growth factor 14
FMR1 fragile X mental retardation 1
FRAXA fragile site, folic acid type, rare, fra(X)(q27.3) A (macroorchidism, mental retardation)
ITPR1 inositol 1,4,5-trisphosphate receptor, type 1
KCND3 potassium channel, voltage gated Shal related subfamily D, member 3
PRKCG protein kinase C, gamma
SCA18 spinocerebellar ataxia 18 (sensory with neurogenic muscular atrophy)
SCA21 spinocerebellar ataxia 21