NPAP1

From LncRNAWiki
Revision as of 03:54, 7 November 2018 by Huma (talk | contribs) (Created page with " ==Annotation== ===Name=== NPAP1 ===Alias=== NA ===Disease=== Disease: angelman syndrome [http://www.ncbi.nlm.nih.gov/pubmed/17337158 (PMID:17337158)] Dysfunction type: ex...")
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Annotation

Name

NPAP1

Alias

NA

Disease

Disease: angelman syndrome (PMID:17337158)

Dysfunction type: expression

Description: C15orf2 and a novel noncoding transcript from the Prader-Willi/Angelman syndrome region show monoallelic expression in fetal brain.


Function

Function Mechanism: NA (PMID:17337158)

Biological Process: pathogenic process

Description: NA

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