LOC110121295 (-)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 110121295 |
| Gene name | - |
| Gene symbol | LOC110121295 |
| Synonyms (NCBI Gene) |
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| Chromosome | 7 |
| Chromosome location | 7q |
| Summary | This locus, which is located in the split-hand/split-foot malformation 1 (SHFM1) region on chromosome 7, represents a conserved genomic element that can function as an enhancer. It can activate a minimal Hsp68 promoter coupled to a reporter gene in branch |
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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 LOC110121295 across shared curated disease and pathway associations.
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Diseases Linked via Similar Genes
Diseases curated for genes most similar to LOC110121295 (see Related Genes above), that are NOT already directly curated for LOC110121295 itself -- a lead worth checking, not a confirmed association.
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