LOC106783508 (-)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 106783508 |
| Gene name | - |
| Gene symbol | LOC106783508 |
| Synonyms (NCBI Gene) |
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| Chromosome | 11 |
| Chromosome location | 11p15.5 |
| Summary | This region, which is poorly conserved between human and mouse at the sequence level, and which is located in an intron of the imprinted KCNQ1 (potassium channel, voltage gated KQT-like subfamily Q, member 1) gene on chromosome 11, can function as an enha |
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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 LOC106783508 across shared curated disease and pathway associations.
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Diseases Linked via Similar Genes
Diseases curated for genes most similar to LOC106783508 (see Related Genes above), that are NOT already directly curated for LOC106783508 itself -- a lead worth checking, not a confirmed association.
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