116HG
Contents
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