Anion exchange transporter is a protein that in humans is encoded by the SLC26A7 gene.[5][6][7][8]
Function
editThis gene is one member of a family of sulfate/anion transporter genes. Family members are well conserved in their genomic (number and size of exons) and protein (aa length among species) structures yet have markedly different tissue expression patterns. This gene has abundant and specific expression in the kidney. Splice variants that use both alternate transcription initiation and polyadenylation sites have been described for this gene.[8]
See also
editReferences
edit- ^ a b c GRCh38: Ensembl release 89: ENSG00000147606 – Ensembl, May 2017
- ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000040569 – Ensembl, May 2017
- ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ Lohi H, Kujala M, Makela S, Lehtonen E, Kestila M, Saarialho-Kere U, Markovich D, Kere J (April 2002). "Functional characterization of three novel tissue-specific anion exchangers SLC26A7, -A8, and -A9". The Journal of Biological Chemistry. 277 (16): 14246–54. doi:10.1074/jbc.M111802200. PMID 11834742.
- ^ Vincourt JB, Jullien D, Kossida S, Amalric F, Girard JP (February 2002). "Molecular cloning of SLC26A7, a novel member of the SLC26 sulfate/anion transporter family, from high endothelial venules and kidney". Genomics. 79 (2): 249–56. doi:10.1006/geno.2002.6689. PMID 11829495.
- ^ Xu J, Worrell RT, Li HC, Barone SL, Petrovic S, Amlal H, Soleimani M (April 2006). "Chloride/bicarbonate exchanger SLC26A7 is localized in endosomes in medullary collecting duct cells and is targeted to the basolateral membrane in hypertonicity and potassium depletion". Journal of the American Society of Nephrology. 17 (4): 956–67. doi:10.1681/ASN.2005111174. PMID 16524946.
- ^ a b "Entrez Gene: SLC26A7 solute carrier family 26, member 7".
Further reading
edit- Markovich D (October 2001). "Physiological roles and regulation of mammalian sulfate transporters". Physiological Reviews. 81 (4): 1499–533. doi:10.1152/physrev.2001.81.4.1499. PMID 11581495. S2CID 30942862.
- Petrovic S, Ju X, Barone S, Seidler U, Alper SL, Lohi H, Kere J, Soleimani M (June 2003). "Identification of a basolateral Cl-/HCO3- exchanger specific to gastric parietal cells". American Journal of Physiology. Gastrointestinal and Liver Physiology. 284 (6): G1093–103. doi:10.1152/ajpgi.00454.2002. PMID 12736153.
- Petrovic S, Barone S, Xu J, Conforti L, Ma L, Kujala M, Kere J, Soleimani M (January 2004). "SLC26A7: a basolateral Cl-/HCO3- exchanger specific to intercalated cells of the outer medullary collecting duct". American Journal of Physiology. Renal Physiology. 286 (1): F161–9. doi:10.1152/ajprenal.00219.2003. PMID 12965893. S2CID 25003214.
- Barone S, Amlal H, Xu J, Kujala M, Kere J, Petrovic S, Soleimani M (August 2004). "Differential regulation of basolateral Cl-/HCO3- exchangers SLC26A7 and AE1 in kidney outer medullary collecting duct". Journal of the American Society of Nephrology. 15 (8): 2002–11. doi:10.1097/01.ASN.0000135060.83250.07. PMID 15284286.
- Kujala M, Tienari J, Lohi H, Elomaa O, Sariola H, Lehtonen E, Kere J (2006). "SLC26A6 and SLC26A7 anion exchangers have a distinct distribution in human kidney". Nephron Experimental Nephrology. 101 (2): e50–8. doi:10.1159/000086345. PMID 15956810. S2CID 26671784.
This article incorporates text from the United States National Library of Medicine, which is in the public domain.
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