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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Genes

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