Mitochondrial Diseases Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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19 genes associated with the Mitochondrial Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
AARS2 alanyl-tRNA synthetase 2, mitochondrial
ACADM acyl-CoA dehydrogenase, C-4 to C-12 straight chain
FAS Fas cell surface death receptor
GSTM1 glutathione S-transferase mu 1
MT-CYB cytochrome b
MT-ND6 NADH dehydrogenase, subunit 6 (complex I)
MTIF3 mitochondrial translational initiation factor 3
MTO1 mitochondrial tRNA translation optimization 1
OGG1 8-oxoguanine DNA glycosylase
POLG polymerase (DNA directed), gamma
PTEN phosphatase and tensin homolog
PTPN11 protein tyrosine phosphatase, non-receptor type 11
RMND1 required for meiotic nuclear division 1 homolog (S. cerevisiae)
SLC25A12 solute carrier family 25 (aspartate/glutamate carrier), member 12
TRL-TAG1-1 transfer RNA-Leu (TAG) 1-1
TYMP thymidine phosphorylase
VARS2 valyl-tRNA synthetase 2, mitochondrial