SLC5A1
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| Solute carrier family 5 (sodium/glucose cotransporter), member 1
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| Identifiers | ||||||||||||||
| Symbol(s) | SLC5A1; D22S675; NAGT; SGLT1 | |||||||||||||
| External IDs | OMIM: 182380 MGI: 107678 Homologene: 55456 | |||||||||||||
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| RNA expression pattern | ||||||||||||||
| Orthologs | ||||||||||||||
| Human | Mouse | |||||||||||||
| Entrez | 6523 | 20537 | ||||||||||||
| Ensembl | ENSG00000100170 | ENSMUSG00000011034 | ||||||||||||
| Uniprot | P13866 | O70122 | ||||||||||||
| Refseq | NM_000343 (mRNA) NP_000334 (protein) | NM_019810 (mRNA) NP_062784 (protein) | ||||||||||||
| Location | Chr 22: 30.77 - 30.84 Mb | Chr 5: 33.42 - 33.48 Mb | ||||||||||||
| Pubmed search | [2] | [3] | ||||||||||||
Solute carrier family 5 (sodium/glucose cotransporter), member 1, also known as SLC5A1, is a human gene.[1]
Glucose transporters are integral membrane proteins that mediate the transport of glucose and structurally-related substances across cellular membranes. Two families of glucose transporter have been identified: the facilitated-diffusion glucose transporter family (GLUT family), also known as 'uniporters,' and the sodium-dependent glucose transporter family (SGLT family), also known as 'cotransporters' or 'symporters' (Wright et al., 1994). The SLC5A1 gene encodes a protein that is involved in the active transport of glucose and galactose into eukaryotic and some prokaryotic cells.[supplied by OMIM][1]
See also
References
Further reading
- Wright EM, Loo DD, Panayotova-Heiermann M, et al. (1995). "'Active' sugar transport in eukaryotes.". J. Exp. Biol. 196: 197-212. PMID 7823022.
- Wright EM, Turk E, Martin MG (2003). "Molecular basis for glucose-galactose malabsorption.". Cell Biochem. Biophys. 36 (2-3): 115-21. PMID 12139397.
- Anderson NL, Anderson NG (2003). "The human plasma proteome: history, character, and diagnostic prospects.". Mol. Cell Proteomics 1 (11): 845-67. PMID 12488461.
- Turk E, Zabel B, Mundlos S, et al. (1991). "Glucose/galactose malabsorption caused by a defect in the Na+/glucose cotransporter.". Nature 350 (6316): 354-6. doi:10.1038/350354a0. PMID 2008213.
- Hediger MA, Turk E, Wright EM (1989). "Homology of the human intestinal Na+/glucose and Escherichia coli Na+/proline cotransporters.". Proc. Natl. Acad. Sci. U.S.A. 86 (15): 5748-52. PMID 2490366.
- Delézay O, Baghdiguian S, Fantini J (1995). "The development of Na(+)-dependent glucose transport during differentiation of an intestinal epithelial cell clone is regulated by protein kinase C.". J. Biol. Chem. 270 (21): 12536-41. PMID 7759499.
- Turk E, Martín MG, Wright EM (1994). "Structure of the human Na+/glucose cotransporter gene SGLT1.". J. Biol. Chem. 269 (21): 15204-9. PMID 8195156.
- Turk E, Klisak I, Bacallao R, et al. (1993). "Assignment of the human Na+/glucose cotransporter gene SGLT1 to chromosome 22q13.1.". Genomics 17 (3): 752-4. doi:10.1006/geno.1993.1399. PMID 8244393.
- Martín MG, Turk E, Lostao MP, et al. (1996). "Defects in Na+/glucose cotransporter (SGLT1) trafficking and function cause glucose-galactose malabsorption.". Nat. Genet. 12 (2): 216-20. doi:10.1038/ng0296-216. PMID 8563765.
- Turk E, Kerner CJ, Lostao MP, Wright EM (1996). "Membrane topology of the human Na+/glucose cotransporter SGLT1.". J. Biol. Chem. 271 (4): 1925-34. PMID 8567640.
- Lam JT, Martín MG, Turk E, et al. (1999). "Missense mutations in SGLT1 cause glucose-galactose malabsorption by trafficking defects.". Biochim. Biophys. Acta 1453 (2): 297-303. PMID 10036327.
- Dunham I, Shimizu N, Roe BA, et al. (1999). "The DNA sequence of human chromosome 22.". Nature 402 (6761): 489-95. doi:10.1038/990031. PMID 10591208.
- Obermeier S, Hüselweh B, Tinel H, et al. (2001). "Expression of glucose transporters in lactating human mammary gland epithelial cells.". European journal of nutrition 39 (5): 194-200. PMID 11131365.
- Kasahara M, Maeda M, Hayashi S, et al. (2001). "A missense mutation in the Na(+)/glucose cotransporter gene SGLT1 in a patient with congenital glucose-galactose malabsorption: normal trafficking but inactivation of the mutant protein.". Biochim. Biophys. Acta 1536 (2-3): 141-7. PMID 11406349.
- Roll P, Massacrier A, Pereira S, et al. (2002). "New human sodium/glucose cotransporter gene (KST1): identification, characterization, and mutation analysis in ICCA (infantile convulsions and choreoathetosis) and BFIC (benign familial infantile convulsions) families.". Gene 285 (1-2): 141-8. PMID 12039040.
- Ikari A, Nakano M, Kawano K, Suketa Y (2002). "Up-regulation of sodium-dependent glucose transporter by interaction with heat shock protein 70.". J. Biol. Chem. 277 (36): 33338-43. doi:10.1074/jbc.M200310200. PMID 12082088.
- 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.
Template:Membrane-protein-stub This article incorporates text from the United States National Library of Medicine, which is in the public domain.
Acknowledgement and Attribution Regarding Sources of Content
Some of the initial content on this page may be incorporated in part from copyleft sources in the public domain including wikis such as Wikipedia and AskDrWiki. Drug information for patients came from the The National Library of Medicine. Infectious disease information may have come from the Centers for Disease Control (CDC). Differential Diagnoses are drawn from clinicians as well as an amalgamation of 3 sources: 1.The Disease Database; 2. Kahan, Scott, Smith, Ellen G. In A Page: Signs and Symptoms. Malden, Massachusetts: Blackwell Publishing, 2004:3; 3. Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:7 .
