Spinocerebellar Tract Degeneration Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C1866751
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Genes

15 genes associated with the disease Spinocerebellar Tract Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
APOE apolipoprotein E
ATXN1 ataxin 1
ATXN2 ataxin 2
ATXN3 ataxin 3
BEAN1 brain expressed, associated with NEDD4, 1
CACNA1A calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
CRH corticotropin releasing hormone
FXN frataxin
GCLC glutamate-cysteine ligase, catalytic subunit
GJB1 gap junction protein, beta 1, 32kDa
PLP1 proteolipid protein 1
TDP1 tyrosyl-DNA phosphodiesterase 1
TGFB1 transforming growth factor, beta 1
TK2 thymidine kinase 2, mitochondrial
TTBK2 tau tubulin kinase 2