Delirium Gene Set

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

15 genes associated with the Delirium phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
ABCB1 ATP-binding cassette, sub-family B (MDR/TAP), member 1
ABCG2 ATP-binding cassette, sub-family G (WHITE), member 2 (Junior blood group)
APOE apolipoprotein E
CNR1 cannabinoid receptor 1 (brain)
COMT catechol-O-methyltransferase
CXCL8 chemokine (C-X-C motif) ligand 8
CYP3A5 cytochrome P450, family 3, subfamily A, polypeptide 5
DRD2 dopamine receptor D2
DRD3 dopamine receptor D3
IL6 interleukin 6
IL6R interleukin 6 receptor
MTNR1B melatonin receptor 1B
NR3C1 nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor)
SLC6A3 solute carrier family 6 (neurotransmitter transporter), member 3
SOAT1 sterol O-acyltransferase 1