Mitochondrial Diseases Gene Set
Genes
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)
|
|
MT-TK
|
tRNA
|
|
MT-TL1
|
tRNA
|
|
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
|
