116HG

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Revision as of 07:38, 2 November 2018 by Fatima (talk | contribs) (Created page with "==Annotation== ===Name=== 116HG ===Alias=== NA ===Disease=== Disease: Prader-Willi syndrome [http://www.ncbi.nlm.nih.gov/pubmed/24624135 (PMID:24624135)] Dysfunction type:...")
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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

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