Glucose Metabolism Disorders Gene Set

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

36 genes associated with the Glucose Metabolism Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
ABCC8 ATP-binding cassette, sub-family C (CFTR/MRP), member 8
ADIPOQ adiponectin, C1Q and collagen domain containing
ADM adrenomedullin
ADRB2 adrenoceptor beta 2, surface
ADRB3 adrenoceptor beta 3
APOA5 apolipoprotein A-V
APOE apolipoprotein E
CAPN10 calpain 10
CDKAL1 CDK5 regulatory subunit associated protein 1-like 1
CDKN2A cyclin-dependent kinase inhibitor 2A
CDKN2B cyclin-dependent kinase inhibitor 2B (p15, inhibits CDK4)
FABP2 fatty acid binding protein 2, intestinal
GCK glucokinase (hexokinase 4)
GCKR glucokinase (hexokinase 4) regulator
GYS1 glycogen synthase 1 (muscle)
HHEX hematopoietically expressed homeobox
HNF1B HNF1 homeobox B
HNF4A hepatocyte nuclear factor 4, alpha
IDE insulin-degrading enzyme
IGF2BP2 insulin-like growth factor 2 mRNA binding protein 2
IL6 interleukin 6
IRS1 insulin receptor substrate 1
KCNJ11 potassium channel, inwardly rectifying subfamily J, member 11
LEPR leptin receptor
LIPC lipase, hepatic
OPRM1 opioid receptor, mu 1
PPARA peroxisome proliferator-activated receptor alpha
PPARG peroxisome proliferator-activated receptor gamma
PPARGC1A peroxisome proliferator-activated receptor gamma, coactivator 1 alpha
SH2B1 SH2B adaptor protein 1
SLC2A1 solute carrier family 2 (facilitated glucose transporter), member 1
SLC30A8 solute carrier family 30 (zinc transporter), member 8
TCF7L2 transcription factor 7-like 2 (T-cell specific, HMG-box)
TNF tumor necrosis factor
UCP2 uncoupling protein 2 (mitochondrial, proton carrier)
WFS1 Wolfram syndrome 1 (wolframin)