LOC107048982 (-)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 107048982 |
| Gene name | - |
| Gene symbol | LOC107048982 |
| Synonyms (NCBI Gene) |
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| Chromosome | X |
| Chromosome location | - |
| Summary | This region contains an origin of DNA replication located greater than 50 kb upstream of the FMR1 (fragile X mental retardation 1) gene. A C vs T single nucleotide polymorphism in this sequence (rs45631657) influences activity of this origin, with the C 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 LOC107048982 across shared curated disease and pathway associations.
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Diseases Linked via Similar Genes
Diseases curated for genes most similar to LOC107048982 (see Related Genes above), that are NOT already directly curated for LOC107048982 itself -- a lead worth checking, not a confirmed association.
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