| MTND5 | OKDB#: 5834 |
| Symbols: | ND5 | Species: | human | ||
| Synonyms: | MTND5 | Locus: |
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| General Comment |
non-nuclear////////////////Heteroplasmic mutations in the MTND5 gene can result in several different mitochondrial disorders, including Leber hereditary optic neuropathy (LHON; 535000), MELAS syndrome (540000), Leigh syndrome (256000), and complex I deficiency (252010).
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| General function | Enzyme | ||||
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| Cellular localization | Mitochondrial | ||||
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| Ovarian localization | Oocyte | ||||
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| Mutations | 0 mutations | ||||
| Genomic Region | show genomic region | ||||
| Phenotypes and GWAS | show phenotypes and GWAS | ||||
| Links |
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| created: | Aug. 4, 2020, 1:44 p.m. | by: |
system email:
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| last update: | Aug. 4, 2020, 1:46 p.m. | by: | hsueh email: |
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