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Rabu, 27 Desember 2017

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A new splice-site mutation in SLC12A6 causing Andermann syndrome ...
src: jnnp.bmj.com

Solute carrier family 12 member 6 is a protein that in humans is encoded by the SLC12A6 gene.

This gene is a member of the K-Cl cotransporter (KCC) family. K-Cl cotransporters are integral membrane proteins that lower intracellular chloride concentrations below the electrochemical equilibrium potential. The proteins encoded by this gene are activated by cell swelling induced by hypotonic conditions. Alternate splicing results in multiple transcript variants encoding different isoforms, the most important ones being KCC3a and KCC3b. Mutations in this gene are associated with agenesis of the corpus callosum with peripheral neuropathy.


Video SLC12A6



See also

  • Solute carrier family

Maps SLC12A6



References


Journal of Neurology, Neurosurgery, and Psychiatry | JNNP's ...
src: f1.media.brightcove.com


External links

  • GeneReview/NIH/UW entry on Hereditary Motor and Sensory Neuropathy with Agenesis of the Corpus Callosum

Alternative pre-mRNA splicing switches modulate gene expression in ...
src: www.bloodjournal.org


Further reading

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


Source of the article : Wikipedia

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