| LncRNA Information | ||||||
|---|---|---|---|---|---|---|
| ID | EL0001 | Name | 116HG | Aliases | N/A | |
| Species | Homo sapiens | Chromosome | 15 | Start site | N/A | |
| End site | N/A | Chain | N/A | Exon NO. | N/A | |
| Assembly | N/A | Class | N/A | NCBI accession | N/A | |
| Ensembl | N/A | Sequence | N/A | |||
| Disease | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Disease | Method | Sample | Expression pattern | Dysfunction type | Description | PMID | Source | ||
| Prader-Willi syndrome | N/A | N/A | N/A | regulation | Long ncRNA 116HG has been shown to play a role in the development of Prader–Willi syndrome (PWS) (Powell et al., 2013). | 24624135 | LncRNADisease | ||