Spinocerebellar Ataxia 17 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:C564616
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Genes

9 genes/proteins associated with the disease Spinocerebellar Ataxia 17 from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
ATP5B ATP synthase, H+ transporting, mitochondrial F1 complex, beta polypeptide 2.88009
HMOX1 heme oxygenase 1 2.88009
HYOU1 hypoxia up-regulated 1 2.88009
P4HB prolyl 4-hydroxylase, beta polypeptide 2.88009
NQO1 NAD(P)H dehydrogenase, quinone 1 2.88009
PDIA3 protein disulfide isomerase family A, member 3 2.88009
TBP TATA box binding protein 2.88009
HSPA5 heat shock 70kDa protein 5 (glucose-regulated protein, 78kDa) 2.88009
HSPA8 heat shock 70kDa protein 8 2.88009