Dystonic Disorders 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:D020821
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20 genes/proteins associated with the disease Dystonic Disorders from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
ALDH5A1 aldehyde dehydrogenase 5 family, member A1 2.88009
THAP1 THAP domain containing, apoptosis associated protein 1 2.88009
TOR1A torsin family 1, member A (torsin A) 2.88009
GNAL guanine nucleotide binding protein (G protein), alpha activating activity polypeptide, olfactory type 2.88009
GLRA1 glycine receptor, alpha 1 2.88009
PRKRA protein kinase, interferon-inducible double stranded RNA dependent activator 2.88009
SLC22A2 solute carrier family 22 (organic cation transporter), member 2 1.80038
PRL prolactin 1.40897
HTR2C 5-hydroxytryptamine (serotonin) receptor 2C, G protein-coupled 1.38752
KCNH2 potassium channel, voltage gated eag related subfamily H, member 2 1.31119
HTR2A 5-hydroxytryptamine (serotonin) receptor 2A, G protein-coupled 1.30117
DRD2 dopamine receptor D2 1.27193
DRD1 dopamine receptor D1 1.27193
CYP2D6 cytochrome P450, family 2, subfamily D, polypeptide 6 1.2707
GAD1 glutamate decarboxylase 1 (brain, 67kDa) 1.20493
SC5D sterol-C5-desaturase 1.11843
HMGCS1 3-hydroxy-3-methylglutaryl-CoA synthase 1 (soluble) 1.10033
CYP3A4 cytochrome P450, family 3, subfamily A, polypeptide 4 1.0766
CAMK2A calcium/calmodulin-dependent protein kinase II alpha 1.05936
CAT catalase 1.01174