LOC109504727 (-)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 109504727 |
| Gene name | - |
| Gene symbol | LOC109504727 |
| Synonyms (NCBI Gene) |
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| Chromosome | 20 |
| Chromosome location | 20p13 |
| Summary | This biological region is found within an intron of the NOP56 ribonucleoprotein gene, and is just upstream of microRNA 1292, on the p arm of chromosome 20. This region contains a GGCCTG hexanucleotide repeat, and expansions of this repeat are associated w |
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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 LOC109504727 across shared curated disease and pathway associations.
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Diseases Linked via Similar Genes
Diseases curated for genes most similar to LOC109504727 (see Related Genes above), that are NOT already directly curated for LOC109504727 itself -- a lead worth checking, not a confirmed association.
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