116HG

From LncRNAWiki
Jump to: navigation, search

Annotation

Name

116HG

Alias

NA

Disease

Disease: Prader-Willi syndrome (PMID:24624135)

Dysfunction type: regulation

Description: Long ncRNA 116HG has been shown to play a role in the development of Prader–Willi syndrome (PWS) (Powell et al., 2013).


Function

Function Mechanism: transcriptional regulation (PMID:24624135)

Biological Process: pathogenic process

Description: NA