TSNAX-DISC1 (TSNAX-DISC1 readthrough (NMD candidate))
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 100303453 |
| Gene name | TSNAX-DISC1 readthrough (NMD candidate) |
| Gene symbol | TSNAX-DISC1 |
| Synonyms (NCBI Gene) |
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| Chromosome | 1 |
| Chromosome location | 1q42.2 |
| Summary | This gene represents naturally occurring read-through transcription between the neighboring TSNAX (translin-associated factor X) and DISC1 (disrupted in schizophrenia 1) genes on chromosome 1. Alternative splicing results in multiple transcript variants, |
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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 TSNAX-DISC1 across shared curated disease and pathway associations.
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Diseases Linked via Similar Genes
Diseases curated for genes most similar to TSNAX-DISC1 (see Related Genes above), that are NOT already directly curated for TSNAX-DISC1 itself -- a lead worth checking, not a confirmed association.
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