| MT-ND4L | OKDB#: 5844 |
| Symbols: | ND4L | Species: | human | ||
| Synonyms: | MTND4L | Locus: |
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OMIM
Entrez Gene
Mammalian Reproductive Genetics Endometrium Database Resource Orthologous Genes UCSC Genome Browser GEO Profiles new! Amazonia (transcriptome data) new! R-L INTERACTIONS MGI |
| General Comment |
non-nuclear //////Approximately 90% of Leber optic atrophy (LHON; 535000) cases are caused by 3460A (516000.0001), 11778A (516003.0001), or 14484C (516006.0001) mtDNA mutations.
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| Cellular localization | Mitochondrial | ||||
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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: | Sept. 2, 2020, 10:35 a.m. | by: |
system email:
home page: |
| last update: | Sept. 2, 2020, 10:38 a.m. | by: | hsueh email: |
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