Neurotic Disorders Gene Set

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

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

Symbol Name
ACE angiotensin I converting enzyme
AGT angiotensinogen (serpin peptidase inhibitor, clade A, member 8)
APOE apolipoprotein E
BDNF brain-derived neurotrophic factor
CNR1 cannabinoid receptor 1 (brain)
COMT catechol-O-methyltransferase
CRHR1 corticotropin releasing hormone receptor 1
CRHR2 corticotropin releasing hormone receptor 2
CRP C-reactive protein, pentraxin-related
DAOA D-amino acid oxidase activator
DRD2 dopamine receptor D2
DRD4 dopamine receptor D4
DTNBP1 dystrobrevin binding protein 1
ESR1 estrogen receptor 1
GABRA2 gamma-aminobutyric acid (GABA) A receptor, alpha 2
GABRA3 gamma-aminobutyric acid (GABA) A receptor, alpha 3
GABRA6 gamma-aminobutyric acid (GABA) A receptor, alpha 6
GABRG2 gamma-aminobutyric acid (GABA) A receptor, gamma 2
GAD1 glutamate decarboxylase 1 (brain, 67kDa)
GAD2 glutamate decarboxylase 2 (pancreatic islets and brain, 65kDa)
GPC6 glypican 6
HTR1A 5-hydroxytryptamine (serotonin) receptor 1A, G protein-coupled
HTR2A 5-hydroxytryptamine (serotonin) receptor 2A, G protein-coupled
MAOA monoamine oxidase A
MDGA2 MAM domain containing glycosylphosphatidylinositol anchor 2
NKAIN2 Na+/K+ transporting ATPase interacting 2
NRG1 neuregulin 1
PDE4D phosphodiesterase 4D, cAMP-specific
PLXNA2 plexin A2
RGS1 regulator of G-protein signaling 1
SLC5A4 solute carrier family 5 (glucose activated ion channel), member 4
SLC6A4 solute carrier family 6 (neurotransmitter transporter), member 4