tardive dyskinesia Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description the involuntary movements are tardive, meaning they have a slow or belated onset (Human Phenotype Ontology, HP_0040141)
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Genes

17 genes associated with the disease tardive dyskinesia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
CYP17A1 cytochrome P450, family 17, subfamily A, polypeptide 1
CYP1A2 cytochrome P450, family 1, subfamily A, polypeptide 2
CYP2D6 cytochrome P450, family 2, subfamily D, polypeptide 6
CYP3A4 cytochrome P450, family 3, subfamily A, polypeptide 4
CYP3A5 cytochrome P450, family 3, subfamily A, polypeptide 5
DRD2 dopamine receptor D2
DRD3 dopamine receptor D3
DRD4 dopamine receptor D4
GSTM1 glutathione S-transferase mu 1
GSTT1 glutathione S-transferase theta 1
HTR2A 5-hydroxytryptamine (serotonin) receptor 2A, G protein-coupled
HTR2C 5-hydroxytryptamine (serotonin) receptor 2C, G protein-coupled
NR4A1 nuclear receptor subfamily 4, group A, member 1
PGP phosphoglycolate phosphatase
SLC6A4 solute carrier family 6 (neurotransmitter transporter), member 4
SOD2 superoxide dismutase 2, mitochondrial
TPH1 tryptophan hydroxylase 1