Combat Disorders Gene Set

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

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

Symbol Name
APOE apolipoprotein E
BDNF brain-derived neurotrophic factor
DBH dopamine beta-hydroxylase (dopamine beta-monooxygenase)
DRD2 dopamine receptor D2
FAAH fatty acid amide hydrolase
GABRB3 gamma-aminobutyric acid (GABA) A receptor, beta 3
MAOB monoamine oxidase B
NOS1AP nitric oxide synthase 1 (neuronal) adaptor protein
NR3C1 nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor)
SLC1A1 solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1
SLC6A4 solute carrier family 6 (neurotransmitter transporter), member 4