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