ENST00000436681

From LncRNAWiki
Revision as of 08:02, 6 November 2018 by Fatima (talk | contribs) (Created page with "==Annotation== ===Name=== ENST00000436681 ===Alias=== AP000552.1 ===Disease=== Disease: congenital heart defect [http://www.ncbi.nlm.nih.gov/pubmed/27035723 (PMID:27035723)]...")
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Annotation

Name

ENST00000436681

Alias

AP000552.1

Disease

Disease: congenital heart defect (PMID:27035723)

Dysfunction type: regulation

Description: The lncRNA aberrantly expressed in the plasma of pregnant women with typical fetal CHD may play a key role in the development of CHD and may be used as novel biomarkers for prenatal diagnosis of fetal CHD.


Function

Function Mechanism: NA (PMID:27035723)

Biological Process: pathogenic process

Description: biomarker