STIN2-VNTR (-)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 110806307 |
| Gene name | - |
| Gene symbol | STIN2-VNTR |
| Synonyms (NCBI Gene) |
5HTT-VNTR25HTTVNTRSTin2.10STin2.12STin2.9VNTR2
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| Chromosome | 17 |
| Chromosome location | 17q11.2 |
| Summary | This genomic sequence represents the STin2 enhancer element in an intron of the solute carrier family 6 member 4 (SLC6A4) gene on chromosome 17. It also represents a polymorphic region consisting of a variable number of tandem repeats (VNTR), where each r |
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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 STIN2-VNTR across shared curated disease and pathway associations.
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Diseases Linked via Similar Genes
Diseases curated for genes most similar to STIN2-VNTR (see Related Genes above), that are NOT already directly curated for STIN2-VNTR itself -- a lead worth checking, not a confirmed association.
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