LncRNA Information
ID	EL0002	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	lncRNA	NCBI accession	N/A
Ensembl	N/A	Sequence	N/A	Peptide-related	N/A
CircRNA	N/A	Exosomal	N/A	Structure	N/A

Disease
Disease	Drug/chemo/stress	Method	Sample	Expression pattern	Dysfunction type	Description	PMID
Prader-Willi syndrome		N/A	N/A	N/A	expression	Long ncRNA 116HG has been shown to play a role in the development of Prader–Willi syndrome (PWS) (Powell et al., 2013).	24624135