Detailed information
| LncRNA Name | LINC00339 |
| Variant Type | SNP |
| Variant ID | rs6426749 |
| Species | human |
| Circulating | ✓ |
| Survival | ✕ |
| CeRNA | ✕ |
| Methylation | ✕ |
| Enhancer | ✓ |
| Drug | ✕ |
| Disease/Trait | osteoporosis |
| LncRNA Target Gene | CDC42 |
| Tissue | blood |
| Experiment | dual-luciferase assay and CRISPR/ Cas9 experiments |
| Function Description | Our study provides mechanistic insight into how a noncoding SNP affects osteoporosis by long-range interaction, a finding that could indicate promising therapeutic targets for osteoporosis. |
| Pubmed ID | 29706346 |
| Year | 2018 |
| Title | An Osteoporosis Risk SNP at 1p36.12 Acts as an Allele-Specific Enhancer to Modulate LINC00339 Expression via Long-Range Loop Formation |
| External Links | |
|---|---|
| Links For LINC00339 | GeneCards HGNC NONCODE LncRNAWiki lncrnadb |
| Links For osteoporosis | OMIM Cosmic |
| Links For rs6426749 | dbSNP ClinVar OMIM |