multiple mitochondrial dna deletions Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The presence of multiple deletions of mitochondrial DNA (mtDNA). (Human Phenotype Ontology, HP_0003689)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003689
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Genes

6 genes associated with the multiple mitochondrial dna deletions phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
C10ORF2 chromosome 10 open reading frame 2
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