Detailed information
| LncRNA Name | PVT1 |
| Variant Type | copy number variation |
| Variant ID | PVT1 in intron 1 |
| Species | human |
| Circulating | ✕ |
| Survival | ✓ |
| CeRNA | ✕ |
| Methylation | ✓ |
| Enhancer | ✕ |
| Drug | ✕ |
| Disease/Trait | B-cell lymphoma |
| LncRNA Target Gene | NA |
| Tissue | bone marrow, lymph node, pleural effusion |
| Experiment | qPCR, FISH, ISH etc. |
| Function Description | In addition, not only MYC rearrangement but also PVT1 rearrangement may also be implicated in the disease development of HABCLs with 8q24 abnormalities. |
| Pubmed ID | 23547836 |
| Year | 2013 |
| Title | Deletion or methylation of CDKN2A/2B and PVT1 rearrangement occur frequently in highly aggressive B-cell lymphomas harboring 8q24 abnormality. |
| External Links | |
|---|---|
| Links For PVT1 | GeneCards HGNC NONCODE LncRNAWiki lncrnadb |
| Links For B-cell lymphoma | OMIM Cosmic |
| Links For PVT1 in intron 1 | dbSNP ClinVar OMIM |