Oxidative Phosphorylation Deficiencies Gene Set
Genes
18 genes associated with the disease Oxidative Phosphorylation Deficiencies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
| Symbol |
Name |
|
AIFM1
|
apoptosis-inducing factor, mitochondrion-associated, 1
|
|
ATP5F1D
|
ATP synthase F1 subunit delta
|
|
FOXRED1
|
FAD-dependent oxidoreductase domain containing 1
|
|
GFM1
|
G elongation factor, mitochondrial 1
|
|
MECP2
|
methyl CpG binding protein 2
|
|
MGME1
|
mitochondrial genome maintenance exonuclease 1
|
|
MPV17
|
MpV17 mitochondrial inner membrane protein
|
|
MTFMT
|
mitochondrial methionyl-tRNA formyltransferase
|
|
MTO1
|
mitochondrial tRNA translation optimization 1
|
|
NDUFA1
|
NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 1, 7.5kDa
|
|
NOL3
|
nucleolar protein 3 (apoptosis repressor with CARD domain)
|
|
NOS2
|
nitric oxide synthase 2, inducible
|
|
NUBPL
|
nucleotide binding protein-like
|
|
PNPT1
|
polyribonucleotide nucleotidyltransferase 1
|
|
POLG
|
polymerase (DNA directed), gamma
|
|
PTCD3
|
pentatricopeptide repeat domain 3
|
|
SCO1
|
SCO1 cytochrome c oxidase assembly protein
|
|
SOD2
|
superoxide dismutase 2, mitochondrial
|
