C15orf2

From LncRNAWiki
Revision as of 08:05, 5 November 2018 by Fatima (talk | contribs) (Created page with "==Annotation== ===Name=== C15orf2 ===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

C15orf2

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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