SLC7A2-IT1A/B

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Revision as of 07:49, 5 November 2018 by Nashaiman (talk | contribs) (Created page with "==Annotation== ===Name=== SLC7A2-IT1A/B ===Alias=== NA ===Disease=== Disease: progressive encephalopathy with severe infantile anorexia [http://www.ncbi.nlm.nih.gov/pubmed/2...")
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Annotation

Name

SLC7A2-IT1A/B

Alias

NA

Disease

Disease: progressive encephalopathy with severe infantile anorexia (PMID:23791884)

Dysfunction type: mutation

Description: Genetic variation in lncRNA genes causes disease and influences susceptibility


Function

Function Mechanism: NA (PMID:23791884)

Biological Process: pathogenic process

Description: NA