LOC108510657 (-)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 108510657 |
| Gene name | - |
| Gene symbol | LOC108510657 |
| Synonyms (NCBI Gene) |
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| Chromosome | 9 |
| Chromosome location | 9q21.11 |
| Summary | This biological region is found within an intron of the frataxin (FXN) gene on the q arm of chromosome 9, and contains a GAA trinucleotide repeat. Expansions of this repeat are known to be a cause of Friedreich ataxia. This region is highly polymorphic, a |
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Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
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Related Genes
Genes most often co-reported with LOC108510657 across shared curated disease and pathway associations.
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Diseases Linked via Similar Genes
Diseases curated for genes most similar to LOC108510657 (see Related Genes above), that are NOT already directly curated for LOC108510657 itself -- a lead worth checking, not a confirmed association.
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