Headache Disorders, Secondary Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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Genes

10 genes associated with the Headache Disorders, Secondary phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
ACE angiotensin I converting enzyme
COMT catechol-O-methyltransferase
DRD2 dopamine receptor D2
HTR1A 5-hydroxytryptamine (serotonin) receptor 1A, G protein-coupled
HTR1B 5-hydroxytryptamine (serotonin) receptor 1B, G protein-coupled
HTR2A 5-hydroxytryptamine (serotonin) receptor 2A, G protein-coupled
HTR6 5-hydroxytryptamine (serotonin) receptor 6, G protein-coupled
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
SLC6A4 solute carrier family 6 (neurotransmitter transporter), member 4
TPH2 tryptophan hydroxylase 2