SLC26A6

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Solute carrier family 26, member 6
Identifiers
Symbol(s) SLC26A6; DKFZp586E1422
External IDs OMIM: 610068 MGI2159728 HomoloGene64480
Orthologs
Human Mouse
Entrez 65010 171429
Ensembl n/a ENSMUSG00000023259
Refseq NM_001040454 (mRNA)
NP_001035544 (protein)
NM_134420 (mRNA)
NP_599252 (protein)
Location n/a Chr 9: 108.71 - 108.77 Mb
Pubmed search [1] [2]

Solute carrier family 26, member 6, also known as SLC26A6, is a human gene.[1]

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.[1]

[edit] See also

[edit] References

[edit] Further reading

  • Markovich D (2001). "Physiological roles and regulation of mammalian sulfate transporters.". Physiol. Rev. 81 (4): 1499-533. PMID 11581495. 
  • Ignatovich O, Tomlinson IM, Popov AV, et al. (2000). "Dominance of intrinsic genetic factors in shaping the human immunoglobulin Vlambda repertoire.". J. Mol. Biol. 294 (2): 457-65. doi:10.1006/jmbi.1999.3243. PMID 10610771. 
  • Lohi H, Kujala M, Kerkelä E, et al. (2001). "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. doi:10.1006/geno.2000.6355. PMID 11087667. 
  • Waldegger S, Moschen I, Ramirez A, et al. (2001). "Cloning and characterization of SLC26A6, a novel member of the solute carrier 26 gene family.". Genomics 72 (1): 43-50. doi:10.1006/geno.2000.6445. PMID 11247665. 
  • Xie Q, Welch R, Mercado A, et al. (2002). "Molecular characterization of the murine Slc26a6 anion exchanger: functional comparison with Slc26a1.". Am. J. Physiol. Renal Physiol. 283 (4): F826-38. doi:10.1152/ajprenal.00079.2002. PMID 12217875. 
  • Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899-903. doi:10.1073/pnas.242603899. PMID 12477932. 
  • Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs.". Nat. Genet. 36 (1): 40-5. doi:10.1038/ng1285. PMID 14702039. 
  • Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).". Genome Res. 14 (10B): 2121-7. doi:10.1101/gr.2596504. PMID 15489334. 
  • Chernova MN, Jiang L, Friedman DJ, et al. (2005). "Functional comparison of mouse slc26a6 anion exchanger with human SLC26A6 polypeptide variants: differences in anion selectivity, regulation, and electrogenicity.". J. Biol. Chem. 280 (9): 8564-80. doi:10.1074/jbc.M411703200. PMID 15548529. 
  • Kujala M, Tienari J, Lohi H, et al. (2006). "SLC26A6 and SLC26A7 anion exchangers have a distinct distribution in human kidney.". Nephron Exp. Nephrol. 101 (2): e50-8. doi:10.1159/000086345. PMID 15956810. 
  • Kimura K, Wakamatsu A, Suzuki Y, et al. (2006). "Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes.". Genome Res. 16 (1): 55-65. doi:10.1101/gr.4039406. PMID 16344560. 
  • Shcheynikov N, Wang Y, Park M, et al. (2006). "Coupling modes and stoichiometry of Cl-/HCO3- exchange by slc26a3 and slc26a6.". J. Gen. Physiol. 127 (5): 511-24. doi:10.1085/jgp.200509392. PMID 16606687. 
  • Olsen JV, Blagoev B, Gnad F, et al. (2006). "Global, in vivo, and site-specific phosphorylation dynamics in signaling networks.". Cell 127 (3): 635-48. doi:10.1016/j.cell.2006.09.026. PMID 17081983. 
  • Alper SL, Stewart AK, Chernova MN, et al. (2007). "Anion exchangers in flux: functional differences between human and mouse SLC26A6 polypeptides.". Novartis Found. Symp. 273: 107-19; discussion 119-25, 261-4. PMID 17120764. 

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