abnormality of glycolysis Gene Set
Genes
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
|
