diabetes, type 2; liver disease Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description disease cluster belonging to disease group unknown (Genetic Association Database)
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Genes

40 genes associated with the disease diabetes, type 2; liver disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
ADRB3 adrenoceptor beta 3
ALB albumin
APOA1 apolipoprotein A-I
APOC3 apolipoprotein C-III
CASP9 caspase 9, apoptosis-related cysteine peptidase
CD36 CD36 molecule (thrombospondin receptor)
CTLA4 cytotoxic T-lymphocyte-associated protein 4
CYP1A1 cytochrome P450, family 1, subfamily A, polypeptide 1
CYP2C19 cytochrome P450, family 2, subfamily C, polypeptide 19
CYP2C9 cytochrome P450, family 2, subfamily C, polypeptide 9
CYP2E1 cytochrome P450, family 2, subfamily E, polypeptide 1
CYP3A4 cytochrome P450, family 3, subfamily A, polypeptide 4
GPX1 glutathione peroxidase 1
GPX3 glutathione peroxidase 3
GPX4 glutathione peroxidase 4
GSTM1 glutathione S-transferase mu 1
GSTT1 glutathione S-transferase theta 1
GYS1 glycogen synthase 1 (muscle)
GYS2 glycogen synthase 2 (liver)
HGF hepatocyte growth factor (hepapoietin A; scatter factor)
IGF1 insulin-like growth factor 1 (somatomedin C)
IGF2 insulin-like growth factor 2
INSR insulin receptor
IRS1 insulin receptor substrate 1
IRS2 insulin receptor substrate 2
IRS4 insulin receptor substrate 4
ITGA1 integrin, alpha 1
LEP leptin
LEPR leptin receptor
LPL lipoprotein lipase
MAOB monoamine oxidase B
NOS2 nitric oxide synthase 2, inducible
NOS3 nitric oxide synthase 3 (endothelial cell)
PPARG peroxisome proliferator-activated receptor gamma
RDH5 retinol dehydrogenase 5 (11-cis/9-cis)
SOD1 superoxide dismutase 1, soluble
TNF tumor necrosis factor
TPMT thiopurine S-methyltransferase
UCP1 uncoupling protein 1 (mitochondrial, proton carrier)
UGT1A1 UDP glucuronosyltransferase 1 family, polypeptide A1