Mitochondrial Dna Mutation Gene Set
Genes
22 genes associated with the disease Mitochondrial Dna Mutation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
| Symbol |
Name |
|
ACTB
|
actin, beta
|
|
AQP4
|
aquaporin 4
|
|
CA8
|
carbonic anhydrase VIII
|
|
COQ7
|
coenzyme Q7 homolog, ubiquinone (yeast)
|
|
COX1
|
|
|
COX8A
|
cytochrome c oxidase subunit VIIIA (ubiquitous)
|
|
GJB2
|
gap junction protein, beta 2, 26kDa
|
|
INS
|
insulin
|
|
MT-CYB
|
cytochrome b
|
|
MT-ND2
|
MTND2
|
|
MT-ND3
|
NADH dehydrogenase, subunit 3 (complex I)
|
|
MT-ND4
|
NADH dehydrogenase, subunit 4 (complex I)
|
|
MT-ND6
|
NADH dehydrogenase, subunit 6 (complex I)
|
|
NOTCH3
|
notch 3
|
|
NPTX2
|
neuronal pentraxin II
|
|
PGD
|
phosphogluconate dehydrogenase
|
|
PIK3CA
|
phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit alpha
|
|
PIK3CB
|
phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit beta
|
|
PIK3CD
|
phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit delta
|
|
PIK3CG
|
phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit gamma
|
|
RXRA
|
retinoid X receptor, alpha
|
|
YARS2
|
tyrosyl-tRNA synthetase 2, mitochondrial
|
