Somatoform Disorders Gene Set

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

28 genes associated with the Somatoform Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
ABAT 4-aminobutyrate aminotransferase
COMT catechol-O-methyltransferase
CRH corticotropin releasing hormone
CRHBP corticotropin releasing hormone binding protein
CRHR1 corticotropin releasing hormone receptor 1
DRD4 dopamine receptor D4
EFHC2 EF-hand domain (C-terminal) containing 2
FAAH fatty acid amide hydrolase
GCH1 GTP cyclohydrolase 1
HTR2A 5-hydroxytryptamine (serotonin) receptor 2A, G protein-coupled
IL1A interleukin 1, alpha
IL1B interleukin 1, beta
IL1RN interleukin 1 receptor antagonist
LTA lymphotoxin alpha
MC2R melanocortin 2 receptor (adrenocorticotropic hormone)
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
NR3C1 nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor)
OPRM1 opioid receptor, mu 1
POMC proopiomelanocortin
SERPINA6 serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 6
SLC6A2 solute carrier family 6 (neurotransmitter transporter), member 2
SLC6A3 solute carrier family 6 (neurotransmitter transporter), member 3
SLC6A4 solute carrier family 6 (neurotransmitter transporter), member 4
TNF tumor necrosis factor
TPH1 tryptophan hydroxylase 1
TPH2 tryptophan hydroxylase 2
TRPA1 transient receptor potential cation channel, subfamily A, member 1
TRPV1 transient receptor potential cation channel, subfamily V, member 1