SLC26A6
From Wikipedia, the free encyclopedia
|
Solute carrier family 26, member 6
|
||||||||||||||
| Identifiers | ||||||||||||||
| Symbol(s) | SLC26A6; DKFZp586E1422 | |||||||||||||
| External IDs | OMIM: 610068 MGI: 2159728 HomoloGene: 64480 | |||||||||||||
|
||||||||||||||
| 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:. 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:. 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:. 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:. 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:. 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:. 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:. 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:. 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:. 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:. 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:. 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:. 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.

