| LncRNA Information | ||||||
|---|---|---|---|---|---|---|
| ID | EL0672 | Name | LINC00951 | Aliases | N/A | |
| Species | Homo sapiens | Chromosome | 6 | Start site | 40344345 | |
| End site | 40356006 | Chain | minus | Exon NO. | 3 | |
| Assembly | GRCh38.p7 | Class | lincRNA | NCBI accession | NR_038887 | |
| Ensembl | N/A | Sequence | ||||
| Disease | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Disease | Method | Sample | Expression pattern | Dysfunction type | Description | PMID | Source | ||
| esophageal squamous cell carcinoma | biochemical assays | N/A | N/A | N/A | functional polymorphism rs11752942A>G in lincRNA-uc003opf.1 exon might be a genetic modifier for the development of ESCC. | 23872665 | |||
| Interaction | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Interaction target | Level of interaction | Type of interaction | Description | PMID | Source | ||||
| rs11752942G allele | DNA-RNA | regulation | rs11752942G allele could markedly attenuate the level of lincRNA-uc003opf.1 both in vivo and in vitro by binding micro-RNA-149*, thereby affecting cell proliferation and tumor growth | 23872665 | |||||