mitochondrial myopathy Gene Set

Dataset DISEASES Curated Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A myopathy that is characterized by mitochondrial dysfunction. (Human Disease Ontology, DOID_699)
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Genes

8 genes involed in the disease mitochondrial myopathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
C10ORF2 chromosome 10 open reading frame 2
DNA2 DNA replication helicase/nuclease 2
MGME1 mitochondrial genome maintenance exonuclease 1
POLG polymerase (DNA directed), gamma
POLG2 polymerase (DNA directed), gamma 2, accessory subunit
RRM2B ribonucleotide reductase M2 B (TP53 inducible)
SLC25A4 solute carrier family 25 (mitochondrial carrier; adenine nucleotide translocator), member 4
TYMP thymidine phosphorylase