Detailed information
| LncRNA Name | RP11-362K14.5 (CCSlnc362) |
| Variant Type | SNP |
| Variant ID | rs1317082 |
| Species | human |
| Circulating | ✕ |
| Survival | ✕ |
| CeRNA | ✕ |
| Methylation | ✕ |
| Enhancer | ✕ |
| Drug | ✕ |
| Disease/Trait | colorectal cancer |
| LncRNA Target Gene | miR-4658 |
| Tissue | HCT116 and DLD-1 cell lines |
| Experiment | qRT-PCR; luciferase reporter assays |
| Function Description | The T>C variant of rs1317082 at CCSlnc362 exon 1 created a binding site for miR-4658 to reduce the expression of CCSlnc362 and thus decreased the susceptibility to CRC. |
| Pubmed ID | 30518759 |
| Year | 2018 |
| Title | Variant of SNP rs1317082 at CCSlnc362(RP11-362K14.5) creates a binding site for miR-4658 and diminishes the susceptibility to CRC |
| External Links | |
|---|---|
| Links For RP11-362K14.5 (CCSlnc362) | GeneCards HGNC NONCODE LncRNAWiki lncrnadb |
| Links For colorectal cancer | OMIM Cosmic |
| Links For rs1317082 | dbSNP ClinVar OMIM |