Spinocerebellar Ataxias Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D020754
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Genes

16 genes/proteins associated with the disease Spinocerebellar Ataxias from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
SPTBN2 spectrin, beta, non-erythrocytic 2 2.88009
FOXC1 forkhead box C1 2.88009
PPP2R2B protein phosphatase 2, regulatory subunit B, beta 2.88009
PRKCG protein kinase C, gamma 2.88009
PLEKHG4 pleckstrin homology domain containing, family G (with RhoGef domain) member 4 2.88009
RBM17 RNA binding motif protein 17 2.88009
ATXN1 ataxin 1 2.88009
ATXN2 ataxin 2 2.88009
ATXN7 ataxin 7 2.88009
CACNA1A calcium channel, voltage-dependent, P/Q type, alpha 1A subunit 2.88009
GFI1 growth factor independent 1 transcription repressor 2.88009
CIC capicua transcriptional repressor 2.88009
AFG3L2 AFG3-like AAA ATPase 2 2.88009
ATXN1L ataxin 1-like 2.88009
TTBK2 tau tubulin kinase 2 2.88009
SCA9 spinocerebellar ataxia 9 2.88009