Related LncRNAs |
ID |
lncRNA Name |
Disease |
Method |
Sample |
Expression pattern |
Dysfunction type |
Description |
PMID |
Source |
EL0001 |
116HG |
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
|
EL0556 |
H19 |
Prader-Willi syndrome |
N/A |
N/A |
N/A |
regulation |
Epigenetic deregulation of lncRNAs genes is associated with disease |
23791884 |
LncRNADisease
|
EL0618 |
IPW |
Prader-Willi syndrome |
N/A |
N/A |
N/A |
mutation |
Genetic variation in lncRNA genes causes disease and influences susceptibility |
23791884 |
LncRNADisease
|
EL0618 |
IPW |
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
|
EL0618 |
IPW |
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
|
EL0618 |
IPW |
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
|
EL0885 |
MKRN3-AS1 |
Prader-Willi syndrome |
N/A |
N/A |
N/A |
epigenetics |
ZNF127 and ZNF127AS are imprinted genes that may be associated with some of the clinical features of the polygenic Prader-Willi syndrome. |
10196367 |
LncRNADisease
|
EL0989 |
NPAP1 |
Prader-Willi syndrome |
N/A |
N/A |
N/A |
expression |
C15orf2 and a novel noncoding transcript from the Prader-Willi/Angelman syndrome region show monoallelic expression in fetal brain. |
17337158 |
LncRNADisease
|
EL1224 |
SNHG14 |
Prader-Willi syndrome |
N/A |
N/A |
N/A |
expression |
Prader–Willi and Angelman syndromes, due to UBE3A expression, are affected due to the presence of a 20-kb NAT, which shares complementary sequences of UBE3A |
23781896 |
LncRNADisease
|
|