citalopram Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A racemate comprising equimolar amounts of (R)-citalopram and its enantiomer, escitalopram. It is used as an antidepressant, although only escitalopram is active. (Chemical Entities of Biological Interest Ontology, CHEBI_3723)
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Genes

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

Symbol Name
ABCB1 ATP-binding cassette, sub-family B (MDR/TAP), member 1
CYP2C19 cytochrome P450, family 2, subfamily C, polypeptide 19
CYP2D6 cytochrome P450, family 2, subfamily D, polypeptide 6
CYP3A4 cytochrome P450, family 3, subfamily A, polypeptide 4
CYP3A5 cytochrome P450, family 3, subfamily A, polypeptide 5
HTR1A 5-hydroxytryptamine (serotonin) receptor 1A, G protein-coupled
HTR2A 5-hydroxytryptamine (serotonin) receptor 2A, G protein-coupled
MAOA monoamine oxidase A
NOL4 nucleolar protein 4
RORA RAR-related orphan receptor A
TPH1 tryptophan hydroxylase 1
TPH2 tryptophan hydroxylase 2