STX16-NPEPL1 (STX16-NPEPL1 readthrough (NMD candidate))
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 100534593 |
| Gene name | STX16-NPEPL1 readthrough (NMD candidate) |
| Gene symbol | STX16-NPEPL1 |
| Synonyms (NCBI Gene) |
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| Chromosome | 20 |
| Chromosome location | 20q13.32 |
| Summary | This locus represents naturally occurring read-through transcription between the neighboring syntaxin 16 (STX16) and aminopeptidase-like 1 (NPEPL1) genes on chromosome 20. The read-through transcript is a candidate for nonsense-mediated mRNA decay (NMD), |
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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 STX16-NPEPL1 across shared curated disease and pathway associations.
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Diseases Linked via Similar Genes
Diseases curated for genes most similar to STX16-NPEPL1 (see Related Genes above), that are NOT already directly curated for STX16-NPEPL1 itself -- a lead worth checking, not a confirmed association.
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