Myoclonic 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/C1834570
Similar Terms
Downloads & Tools

Genes

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

Symbol Name
ADCY5 adenylate cyclase 5
ATP1A3 ATPase, Na+/K+ transporting, alpha 3 polypeptide
CACNA1B calcium channel, voltage-dependent, N type, alpha 1B subunit
CAMP cathelicidin antimicrobial peptide
DBH dopamine beta-hydroxylase (dopamine beta-monooxygenase)
DRD2 dopamine receptor D2
GCH1 GTP cyclohydrolase 1
KCTD17 potassium channel tetramerization domain containing 17
LRP2 low density lipoprotein receptor-related protein 2
MCF2L MCF.2 cell line derived transforming sequence-like
NKX2-1 NK2 homeobox 1
POLR1C polymerase (RNA) I polypeptide C, 30kDa
PRRT2 proline-rich transmembrane protein 2
RELN reelin
SGCE sarcoglycan, epsilon
SGCZ sarcoglycan, zeta
SLITRK1 SLIT and NTRK-like family, member 1
TOR1A torsin family 1, member A (torsin A)