multiple chemical sensitivity Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A syndrome that is an adverse physical reaction to low levels of many common chemicals. (Human Disease Ontology, DOID_4661)
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Genes

16 genes associated with the disease multiple chemical sensitivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
CCKBR cholecystokinin B receptor
CYP2C19 cytochrome P450, family 2, subfamily C, polypeptide 19
CYP2C9 cytochrome P450, family 2, subfamily C, polypeptide 9
CYP2D6 cytochrome P450, family 2, subfamily D, polypeptide 6
CYP3A5 cytochrome P450, family 3, subfamily A, polypeptide 5
GSTM1 glutathione S-transferase mu 1
GSTP1 glutathione S-transferase pi 1
GSTT1 glutathione S-transferase theta 1
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
NAT1 N-acetyltransferase 1 (arylamine N-acetyltransferase)
NAT2 N-acetyltransferase 2 (arylamine N-acetyltransferase)
PON1 paraoxonase 1
PON2 paraoxonase 2
SLC6A4 solute carrier family 6 (neurotransmitter transporter), member 4
SOD2 superoxide dismutase 2, mitochondrial
UGT1A1 UDP glucuronosyltransferase 1 family, polypeptide A1