Electron Transport Chain Deficiencies, Mitochondrial Gene Set

Dataset	DisGeNET Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
External Link	https://www.disgenet.org/browser/0/1/0/C0949855
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Genes

10 genes associated with the disease Electron Transport Chain Deficiencies, Mitochondrial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol	Name
COQ9	coenzyme Q9
FOXRED1	FAD-dependent oxidoreductase domain containing 1
MGME1	mitochondrial genome maintenance exonuclease 1
MPV17	MpV17 mitochondrial inner membrane protein
NOL3	nucleolar protein 3 (apoptosis repressor with CARD domain)
NOS2	nitric oxide synthase 2, inducible
NUBPL	nucleotide binding protein-like
POLG	polymerase (DNA directed), gamma
SCO1	SCO1 cytochrome c oxidase assembly protein
SOD2	superoxide dismutase 2, mitochondrial