psychosis Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A condition characterized by changes of personality and thought patterns often accompanied by hallucinations and delusional beliefs. (Human Phenotype Ontology, HP_0000709)
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12 genes associated with the disease psychosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
BDNF brain-derived neurotrophic factor
COMT catechol-O-methyltransferase
DISC1 disrupted in schizophrenia 1
DRD1 dopamine receptor D1
DRD3 dopamine receptor D3
DRD4 dopamine receptor D4
KCNN3 potassium channel, calcium activated intermediate/small conductance subfamily N alpha, member 3
SLC6A3 solute carrier family 6 (neurotransmitter transporter), member 3
SLC6A4 solute carrier family 6 (neurotransmitter transporter), member 4
TGIF1 TGFB-induced factor homeobox 1
TPH1 tryptophan hydroxylase 1
ZNF804A zinc finger protein 804A