CIDeRplusMitochondrial protein MT-ATP6 associated diseases
MT-ATP6 is a mitochondrial gene that belongs to the ATP synthase (or complex V), an enzyme responsible for the final step of oxidative phosphorylation. Mutations of the MT-ATP6 gene are significantly involved in some rare diseases like the NARP syndrome, the various Leigh syndromes, or Leber optic atrophy (LHON).
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Display GraphStatistics
| Interactions | 65 | Proteins/Genes | 9 | Chemical compounds/drugs | 1 |
| Biological Process(GO) | 2 | Phenotype | 13 |
Proteins/Genes
| MT-ATP6 | 13 |
| MT-ATP6-mut | 2 |
| MT-ATP6-n.G8729A | 2 |
| MT-ATP6-p.W48R | 1 |
| MT-ATP6-p.T53I | 1 |
| Phospholipid-translocating ATPase | 1 |
| MT-ATP8 | 1 |
| MT-ATP6-p.L72R | 1 |
| MT-ATP6-p.H90R | 1 |
Biological Process(GO)
| response to oxidative stress | 1 |
| actin-Nrf2 signaling | 1 |
Chemical compounds/drugs
| succinate dehydrogenase product | 1 |