Idiopathic Familial Dystonia Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0393598
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Genes

9 genes associated with the disease Idiopathic Familial Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ALDH5A1 aldehyde dehydrogenase 5 family, member A1
CACNA1A calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
GLRA1 glycine receptor, alpha 1
GNAL guanine nucleotide binding protein (G protein), alpha activating activity polypeptide, olfactory type
KMT2B lysine (K)-specific methyltransferase 2B
PRKRA protein kinase, interferon-inducible double stranded RNA dependent activator
SGCE sarcoglycan, epsilon
THAP1 THAP domain containing, apoptosis associated protein 1
TOR1A torsin family 1, member A (torsin A)