hyperglycemia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003074
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Genes

17 genes associated with the hyperglycemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ABCC8 ATP-binding cassette, sub-family C (CFTR/MRP), member 8
GATA6 GATA binding protein 6
GCK glucokinase (hexokinase 4)
GLI3 GLI family zinc finger 3
GYS2 glycogen synthase 2 (liver)
HNF1A HNF1 homeobox A
INS insulin
INSR insulin receptor
KCNJ11 potassium channel, inwardly rectifying subfamily J, member 11
LMNA lamin A/C
LRPPRC leucine-rich pentatricopeptide repeat containing
PIK3R1 phosphoinositide-3-kinase, regulatory subunit 1 (alpha)
PPARG peroxisome proliferator-activated receptor gamma
PPP1R3A protein phosphatase 1, regulatory subunit 3A
RFX6 regulatory factor X, 6
ZFP57 ZFP57 zinc finger protein
ZMPSTE24 zinc metallopeptidase STE24