pain Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An unpleasant sensory and emotional experience associated with actual or potential tissue damage, or described in terms of such damage. (Human Phenotype Ontology, HP_0012531)
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10 genes associated with the disease pain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
ABCB1 ATP-binding cassette, sub-family B (MDR/TAP), member 1
ADRB2 adrenoceptor beta 2, surface
COMT catechol-O-methyltransferase
GCH1 GTP cyclohydrolase 1
OPRD1 opioid receptor, delta 1
OPRK1 opioid receptor, kappa 1
OPRM1 opioid receptor, mu 1
SCN9A sodium channel, voltage gated, type IX alpha subunit
SLC6A4 solute carrier family 6 (neurotransmitter transporter), member 4
ZNF429 zinc finger protein 429