abnormality of glycolysis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of glycolysis. (Human Phenotype Ontology, HP_0004366)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0004366
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9 genes associated with the abnormality of glycolysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ACAT2 acetyl-CoA acetyltransferase 2
AIFM1 apoptosis-inducing factor, mitochondrion-associated, 1
BCS1L BC1 (ubiquinol-cytochrome c reductase) synthesis-like
GPI glucose-6-phosphate isomerase
LDHA lactate dehydrogenase A
MPC1 mitochondrial pyruvate carrier 1
PC pyruvate carboxylase
PDHX pyruvate dehydrogenase complex, component X
UQCRC2 ubiquinol-cytochrome c reductase core protein II