LOC106799832 (-)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 106799832 |
| Gene name | - |
| Gene symbol | LOC106799832 |
| Synonyms (NCBI Gene) |
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| Chromosome | 22 |
| Chromosome location | 22q11.2 |
| Summary | This region, which is located in an intron of the CECR1 (cat eye syndrome chromosome region, candidate 1) gene on chromosome 22, can function as an enhancer in human Jurkat T cells. The spatially equivalent or corresponding region in mouse, which is not c |
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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 LOC106799832 across shared curated disease and pathway associations.
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Diseases Linked via Similar Genes
Diseases curated for genes most similar to LOC106799832 (see Related Genes above), that are NOT already directly curated for LOC106799832 itself -- a lead worth checking, not a confirmed association.
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