SLC26A6 explained

Solute carrier family 26 member 6 is a protein that in humans is encoded by the SLC26A6 gene.[1] [2] [3] It is an anion-exchanger expressed in the apical membrane of the kidney proximal tubule, the apical membranes of the duct cells in the pancreas, and the villi of the duodenum.[4]

This gene belongs to the solute carrier 26 family, whose members encode anion transporter proteins. This particular family member encodes a protein involved in transporting chloride, oxalate, sulfate and bicarbonate. Several alternatively spliced transcript variants of this gene, encoding distinct isoforms, have been described, but the full-length nature of some of these variants has not been determined.[3]

Associated diseases

Diseases associated with SLC26A6 include sialolithiasis and urolithiasis.[5]

See also

Further reading

Notes and References

  1. Lohi H . Kujala M . Kerkela E . Saarialho-Kere U . Kestila M . Kere J . Mapping of five new putative anion transporter genes in human and characterization of SLC26A6, a candidate gene for pancreatic anion exchanger . Genomics . 70 . 1 . 102–12 . Jan 2001 . 11087667 . 10.1006/geno.2000.6355 .
  2. Waldegger S . Moschen I . Ramirez A . Smith RJ . Ayadi H . Lang F . Kubisch C . Cloning and characterization of SLC26A6, a novel member of the solute carrier 26 gene family . Genomics . 72 . 1 . 43–50 . Mar 2001 . 11247665 . 10.1006/geno.2000.6445 .
  3. Web site: Entrez Gene: SLC26A6 solute carrier family 26, member 6.
  4. Wang. Zhaohui. Tong Wang . Snezana Petrovic . Biguang Tuo . Brigitte Riederer . Sharon Barone . John N. Lorenz . Ursula Seidler . Peter S. Aronson . Manoocher Soleimani . Renal and intestinal transport defects in Slc26a6-null mice. American Journal of Physiology. Cell Physiology. April 2005. 288. 4. 4. C957–C965. 10.1152/ajpcell.00505.2004. 15574486. 23214608 .
  5. Web site: SLC26A6 Gene - GeneCards S26A6 Protein S26A6 Antibody. 2021-05-06. www.genecards.org.