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 | ||