obsessive compulsive disorder Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An anxiety disorder that involves unwanted and repeated thoughts, feelings, ideas, sensations (obsessions), or behaviors that make them feel driven to do something (compulsions). (Human Disease Ontology, DOID_10933)
Similar Terms
Downloads & Tools

Genes

15 genes associated with the disease obsessive compulsive disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
BDNF brain-derived neurotrophic factor
COMT catechol-O-methyltransferase
DRD4 dopamine receptor D4
GRIK2 glutamate receptor, ionotropic, kainate 2
GRIK3 glutamate receptor, ionotropic, kainate 3
GRIN2B glutamate receptor, ionotropic, N-methyl D-aspartate 2B
HTR1B 5-hydroxytryptamine (serotonin) receptor 1B, G protein-coupled
HTR1D 5-hydroxytryptamine (serotonin) receptor 1D, G protein-coupled
HTR2A 5-hydroxytryptamine (serotonin) receptor 2A, G protein-coupled
MAOA monoamine oxidase A
NTRK3 neurotrophic tyrosine kinase, receptor, type 3
SLC1A1 solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1
SLC6A3 solute carrier family 6 (neurotransmitter transporter), member 3
SLC6A4 solute carrier family 6 (neurotransmitter transporter), member 4
TNF tumor necrosis factor