LOC110594336 (-)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 110594336 |
| Gene name | - |
| Gene symbol | LOC110594336 |
| Synonyms (NCBI Gene) |
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| Chromosome | 1 |
| Chromosome location | 1p35.2 |
| Summary | This region is a highly variable minisatellite region that overlaps the serine incorporator 2 (SERINC2) gene on the p arm of chromosome 1. The MS1 (D1S7) minisatellite is a highly unstable GC-rich variable number tandem repeat (VNTR) with a repeat unit le |
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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 LOC110594336 across shared curated disease and pathway associations.
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Diseases Linked via Similar Genes
Diseases curated for genes most similar to LOC110594336 (see Related Genes above), that are NOT already directly curated for LOC110594336 itself -- a lead worth checking, not a confirmed association.
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