hypoglycemic coma Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001325
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Genes

9 genes associated with the hypoglycemic coma 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
ETFA electron-transfer-flavoprotein, alpha polypeptide
ETFB electron-transfer-flavoprotein, beta polypeptide
ETFDH electron-transferring-flavoprotein dehydrogenase
GCK glucokinase (hexokinase 4)
GLUD1 glutamate dehydrogenase 1
HADH hydroxyacyl-CoA dehydrogenase
INSR insulin receptor
SLC16A1 solute carrier family 16 (monocarboxylate transporter), member 1