Mitochondrial Dna Depletion Syndrome Gene Set

Dataset	DisGeNET Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
External Link	https://www.disgenet.org/browser/0/1/0/C2749861
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Genes

14 genes associated with the disease Mitochondrial Dna Depletion Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol	Name
DGUOK	deoxyguanosine kinase
EDAR	ectodysplasin A receptor
MGME1	mitochondrial genome maintenance exonuclease 1
OPA1	optic atrophy 1 (autosomal dominant)
OVOL2	ovo-like zinc finger 2
POLG	polymerase (DNA directed), gamma
RRM2B	ribonucleotide reductase M2 B (TP53 inducible)
SCO2	SCO2 cytochrome c oxidase assembly protein
SLC25A4	solute carrier family 25 (mitochondrial carrier; adenine nucleotide translocator), member 4
SUCLA2	succinate-CoA ligase, ADP-forming, beta subunit
SUCLG1	succinate-CoA ligase, alpha subunit
TFAM	transcription factor A, mitochondrial
TK2	thymidine kinase 2, mitochondrial
TYMP	thymidine phosphorylase