Writer'S Cramp Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A focal dystonia of the fingers, hand, and/or forearm that appears when the affected person attempts to do a task that requires fine motor movements such as writing or playing a musical instrument. (Human Phenotype Ontology, HP_0002356)
External Link https://www.disgenet.org/browser/0/1/0/C4316810
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Genes

25 genes associated with the disease Writer'S Cramp in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ALDH5A1 aldehyde dehydrogenase 5 family, member A1
ANKK1 ankyrin repeat and kinase domain containing 1
ARSG arylsulfatase G
CASR calcium-sensing receptor
CIZ1 CDKN1A interacting zinc finger protein 1
CLCN1 chloride channel, voltage-sensitive 1
COL6A3 collagen, type VI, alpha 3
DRD2 dopamine receptor D2
FTL ferritin, light polypeptide
GCH1 GTP cyclohydrolase 1
GLRA1 glycine receptor, alpha 1
GNA11 guanine nucleotide binding protein (G protein), alpha 11 (Gq class)
GNAL guanine nucleotide binding protein (G protein), alpha activating activity polypeptide, olfactory type
HINT1 histidine triad nucleotide binding protein 1
KCNA1 potassium channel, voltage gated shaker related subfamily A, member 1
KCTD17 potassium channel tetramerization domain containing 17
KMT2B lysine (K)-specific methyltransferase 2B
PRKRA protein kinase, interferon-inducible double stranded RNA dependent activator
PRRT2 proline-rich transmembrane protein 2
SGCE sarcoglycan, epsilon
SLC2A1 solute carrier family 2 (facilitated glucose transporter), member 1
TBC1D24 TBC1 domain family, member 24
TBP TATA box binding protein
THAP1 THAP domain containing, apoptosis associated protein 1
TOR1A torsin family 1, member A (torsin A)