RTEL1-TNFRSF6B (RTEL1-TNFRSF6B readthrough (NMD candidate))
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 100533107 |
| Gene name | RTEL1-TNFRSF6B readthrough (NMD candidate) |
| Gene symbol | RTEL1-TNFRSF6B |
| Synonyms (NCBI Gene) |
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| Chromosome | 20 |
| Chromosome location | 20q13.33 |
| Summary | This locus represents naturally occurring read-through transcription between the neighboring RTEL1 (regulator of telomere elongation helicase 1) and TNFRSF6B (tumor necrosis factor receptor superfamily, member 6b, decoy) genes on chromosome 20. The read-t |
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miRNA
miRNA information provided by mirtarbase database.
2
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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 RTEL1-TNFRSF6B across shared curated disease and pathway associations.
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Diseases Linked via Similar Genes
Diseases curated for genes most similar to RTEL1-TNFRSF6B (see Related Genes above), that are NOT already directly curated for RTEL1-TNFRSF6B itself -- a lead worth checking, not a confirmed association.
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