CIDeRplusMitochondrial protein MT-ND2 associated rare diseases
MT-ND2, a subunit of NADH dehydrogenase (ubiquinone), is located in the mitochondrial inner membrane. Mutations of MT-ND2 are associated with rare mitochondrial diseases like Leigh syndrome and Leber optic atrophy (LHON).
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Display GraphStatistics
| Interactions | 15 | Proteins/Genes | 4 | Chemical compounds/drugs | 0 |
| Biological Process(GO) | 0 | Phenotype | 4 |
Proteins/Genes
| MT-ND2 | 5 |
| MT-ND2-mut | 2 |
| MT-ND2-p.L128Q | 1 |
| MT-ND2-p.I159V | 1 |