Deficiency Of Monooxygenase Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C1291314
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Genes

16 genes associated with the disease Deficiency Of Monooxygenase in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
CFTR cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
CHST14 carbohydrate (N-acetylgalactosamine 4-0) sulfotransferase 14
CYP11B1 cytochrome P450, family 11, subfamily B, polypeptide 1
CYP11B2 cytochrome P450, family 11, subfamily B, polypeptide 2
CYP17A1 cytochrome P450, family 17, subfamily A, polypeptide 1
CYP24A1 cytochrome P450, family 24, subfamily A, polypeptide 1
CYP2B6 cytochrome P450, family 2, subfamily B, polypeptide 6
CYP2R1 cytochrome P450, family 2, subfamily R, polypeptide 1
DOCK11 dedicator of cytokinesis 11
GGCT gamma-glutamylcyclotransferase
GH1 growth hormone 1
PLOD1 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 1
POMC proopiomelanocortin
PPIG peptidylprolyl isomerase G (cyclophilin G)
REN renin
TGM2 transglutaminase 2