CHKB-CPT1B (CHKB-CPT1B readthrough (NMD candidate))
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 386593 |
| Gene name | CHKB-CPT1B readthrough (NMD candidate) |
| Gene symbol | CHKB-CPT1B |
| Synonyms (NCBI Gene) |
CHKL-CPT1BCPT1-MCPT1BCPTI-M
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| Chromosome | 22 |
| Chromosome location | 22q13.33 |
| Summary | The genes CHKB and CPT1B are adjacent on chromosome 22 and read-through transcripts are expressed that include exons from both loci. The read-through transcripts are candidates for nonsense-mediated mRNA decay (NMD) and are unlikely to express proteins. [ |
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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 CHKB-CPT1B across shared curated disease and pathway associations.
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Diseases Linked via Similar Genes
Diseases curated for genes most similar to CHKB-CPT1B (see Related Genes above), that are NOT already directly curated for CHKB-CPT1B itself -- a lead worth checking, not a confirmed association.
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