LncRNA Information
ID	EL0618	Name	IPW	Aliases	NCRNA00002
Species	Homo sapiens	Chromosome	15	Start site	25116545
End site	25122476	Chain	plus	Exon NO.	3
Assembly	GRCh38.p7	Class	N/A	NCBI accession	NR_023915
Ensembl	N/A	Sequence

Disease
Disease	Method	Sample	Expression pattern	Dysfunction type	Description	PMID	Source
Prader-Willi syndrome	N/A	N/A	N/A	mutation	Genetic variation in lncRNA genes causes disease and influences susceptibility	23791884	LncRNADisease
Prader-Willi syndrome	N/A	N/A	N/A	expression	Subsequently, we determined that IPW, along?noncoding?RNA?in the critical region of the PWS locus, is a regulator of the DLK1-DIO3 region, as its overexpression in PWS and parthenogenetic iPSCs resulted in downregulation of MEGs in this locus.?	24816254	LncRNADisease
Prader-Willi syndrome	N/A	N/A	N/A	locus	IPW (Imprinted gene in the Prader-Willi syndrome region) was isolated using the direct selection method and yeast artificial chromosomes localized to the deletion region. the mRNA product of IPW may play a role in the imprinting process.	7849716	LncRNADisease
Prader-Willi syndrome	N/A	N/A	N/A	expression	The Prader-Willi syndrome (PWS) is caused by genomic alterations that inactivate imprinted, paternally expressed genes in human chromosome region 15q11-q13. IPW, a paternally expressed gene cloned from this region, is not expressed in individuals with PWS.	9063754	LncRNADisease