spinocerebellar degeneration Gene Set

Dataset DISEASES Curated Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
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Genes

22 genes involed in the disease spinocerebellar degeneration from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
ABCB7 ATP-binding cassette, sub-family B (MDR/TAP), member 7
AFG3L2 AFG3-like AAA ATPase 2
ATN1 atrophin 1
ATXN1 ataxin 1
ATXN2 ataxin 2
ATXN3 ataxin 3
ATXN7 ataxin 7
BEAN1 brain expressed, associated with NEDD4, 1
C10ORF2 chromosome 10 open reading frame 2
CACNA1A calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
DAGLA diacylglycerol lipase, alpha
EEF2 eukaryotic translation elongation factor 2
FXN frataxin
ITPR1 inositol 1,4,5-trisphosphate receptor, type 1
KCNC3 potassium channel, voltage gated Shaw related subfamily C, member 3
KCND3 potassium channel, voltage gated Shal related subfamily D, member 3
PPP2R2B protein phosphatase 2, regulatory subunit B, beta
PRKCG protein kinase C, gamma
TBP TATA box binding protein
TGM6 transglutaminase 6
TPP1 tripeptidyl peptidase I
TTBK2 tau tubulin kinase 2