psychiatric disorders Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An abnormality of mental functioning including various affective, behavioural, cognitive and perceptual abnormalities. (Human Phenotype Ontology, HP_0000708)
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Genes

71 genes associated with the disease psychiatric disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
ACHE acetylcholinesterase (Yt blood group)
ACTN2 actinin, alpha 2
ADRA2C adrenoceptor alpha 2C
ADRBK2 adrenergic, beta, receptor kinase 2
AUTS2 autism susceptibility candidate 2
CLINT1 clathrin interactor 1
CNTN5 contactin 5
CNTN6 contactin 6
COMT catechol-O-methyltransferase
CORT cortistatin
CRIPT cysteine-rich PDZ-binding protein
CYP2C19 cytochrome P450, family 2, subfamily C, polypeptide 19
CYP2D6 cytochrome P450, family 2, subfamily D, polypeptide 6
DGCR6 DiGeorge syndrome critical region gene 6
DISC1 disrupted in schizophrenia 1
DLG1 discs, large homolog 1 (Drosophila)
DLG2 discs, large homolog 2 (Drosophila)
DRD4 dopamine receptor D4
DRD5 dopamine receptor D5
FKBP5 FK506 binding protein 5
FZD9 frizzled class receptor 9
GABBR1 gamma-aminobutyric acid (GABA) B receptor, 1
GABRD gamma-aminobutyric acid (GABA) A receptor, delta
GABRG3 gamma-aminobutyric acid (GABA) A receptor, gamma 3
GALR1 galanin receptor 1
GALR3 galanin receptor 3
GDF2 growth differentiation factor 2
GLO1 glyoxalase I
GNRHR2 gonadotropin-releasing hormone (type 2) receptor 2, pseudogene
GRIA1 glutamate receptor, ionotropic, AMPA 1
GRIA2 glutamate receptor, ionotropic, AMPA 2
GRIN2A glutamate receptor, ionotropic, N-methyl D-aspartate 2A
GRIN3B glutamate receptor, ionotropic, N-methyl-D-aspartate 3B
GRM5 glutamate receptor, metabotropic 5
GRM7 glutamate receptor, metabotropic 7
GRM8 glutamate receptor, metabotropic 8
HCRTR1 hypocretin (orexin) receptor 1
HTR1B 5-hydroxytryptamine (serotonin) receptor 1B, G protein-coupled
HTR2A 5-hydroxytryptamine (serotonin) receptor 2A, G protein-coupled
IMMP2L IMP2 inner mitochondrial membrane peptidase-like (S. cerevisiae)
IMPA2 inositol(myo)-1(or 4)-monophosphatase 2
NGF nerve growth factor (beta polypeptide)
NIPA1 non imprinted in Prader-Willi/Angelman syndrome 1
NLGN1 neuroligin 1
NOS1AP nitric oxide synthase 1 (neuronal) adaptor protein
NOS2 nitric oxide synthase 2, inducible
NPPC natriuretic peptide C
NPR3 natriuretic peptide receptor 3
NRG3 neuregulin 3
NRXN3 neurexin 3
NSF N-ethylmaleimide-sensitive factor
NTSR1 neurotensin receptor 1 (high affinity)
PLCB4 phospholipase C, beta 4
PLCD1 phospholipase C, delta 1
PPP3CC protein phosphatase 3, catalytic subunit, gamma isozyme
PRODH proline dehydrogenase (oxidase) 1
RTN4R reticulon 4 receptor
S100B S100 calcium binding protein B
SCT secretin
SDK1 sidekick cell adhesion molecule 1
SHMT1 serine hydroxymethyltransferase 1 (soluble)
SLC1A1 solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1
SLC1A2 solute carrier family 1 (glial high affinity glutamate transporter), member 2
SLC6A13 solute carrier family 6 (neurotransmitter transporter), member 13
SLC6A2 solute carrier family 6 (neurotransmitter transporter), member 2
SSTR5 somatostatin receptor 5
TACR1 tachykinin receptor 1
TFIP11 tuftelin interacting protein 11
TRH thyrotropin-releasing hormone
TSNAX translin-associated factor X
VIP vasoactive intestinal peptide