CIDeRplusMitochondrial protein MT-ND5 associated rare diseases
MT-ND5, a subunit of NADH dehydrogenase (ubiquinone), is located in the mitochondrial inner membrane. Mutations of MT-ND5 are associated with rare mitochondrial diseases like Leigh syndrome, Leber optic atrophy (LHON), MELAS, and MERRF.
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| Interactions | 56 | Proteins/Genes | 9 | Chemical compounds/drugs | 0 |
| Biological Process(GO) | 0 | Phenotype | 17 |
Proteins/Genes
| MT-ND5-mut | 12 |
| MT-ND5 | 8 |
| MT-ND5-p.A236T | 3 |
| MT-ND5-p.E145G | 1 |
| MT-ND5-p.M237L | 1 |
| MT-ND5-p.S250C | 1 |
| MT-ND5-p.D393N | 1 |
| MT-ND5-p.N505H | 1 |
| MT-ND5-p.L272P | 1 |