Anoctamin 6: Difference between revisions

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(Created page with '{{Infobox_gene}} '''Anoctamin 6''' is a protein that in humans is encoded by the ANO6 gene. <ref name="entrez"> {{cite web | title = Entrez Gene: Anocta...')
 
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{{cite web
| title = Entrez Gene: Anoctamin 6
| title = Entrez Gene: Anoctamin 6
| url = http://www.ncbi.nlm.nih.gov/gene/196527
| url = https://www.ncbi.nlm.nih.gov/gene/196527
| accessdate = 2017-09-28
| accessdate = 2017-09-28
}}</ref>
}}</ref>

Latest revision as of 08:42, 20 December 2017

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Identifiers
Aliases
External IDsGeneCards: [1]
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

n/a

n/a

RefSeq (protein)

n/a

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Location (UCSC)n/an/a
PubMed searchn/an/a
Wikidata
View/Edit Human

Anoctamin 6 is a protein that in humans is encoded by the ANO6 gene. [1]

Function

This gene encodes a multi-pass transmembrane protein that belongs to the anoctamin family. This protein is an essential component for the calcium-dependent exposure of phosphatidylserine on the cell surface. The scrambling of phospholipid occurs in various biological systems, such as when blood platelets are activated, they expose phosphatidylserine to trigger the clotting system. Mutations in this gene are associated with Scott syndrome. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.

References

  1. "Entrez Gene: Anoctamin 6". Retrieved 2017-09-28.

Further reading


This article incorporates text from the United States National Library of Medicine, which is in the public domain.