Abnormal Involuntary Movement Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description anomaly in movements that occur independent of planning (e.g. reflexive behavior) (Mammalian Phenotype Ontology, MP_0003492)
External Link https://www.disgenet.org/browser/0/1/0/C0392702
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Genes

22 genes associated with the disease Abnormal Involuntary Movement in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
COMT catechol-O-methyltransferase
CREB1 cAMP responsive element binding protein 1
CYP2D6 cytochrome P450, family 2, subfamily D, polypeptide 6
CYP4F3 cytochrome P450, family 4, subfamily F, polypeptide 3
DRD2 dopamine receptor D2
DRD3 dopamine receptor D3
EMD emerin
ERBB4 erb-b2 receptor tyrosine kinase 4
FOXG1 forkhead box G1
GAD1 glutamate decarboxylase 1 (brain, 67kDa)
GPR88 G protein-coupled receptor 88
HTR1A 5-hydroxytryptamine (serotonin) receptor 1A, G protein-coupled
MAOA monoamine oxidase A
MAOB monoamine oxidase B
NR4A1 nuclear receptor subfamily 4, group A, member 1
PANK2 pantothenate kinase 2
PITX3 paired-like homeodomain 3
PPP1R1B protein phosphatase 1, regulatory (inhibitor) subunit 1B
RGS9 regulator of G-protein signaling 9
SOD2 superoxide dismutase 2, mitochondrial
SPTBN2 spectrin, beta, non-erythrocytic 2
TPI1 triosephosphate isomerase 1