SLC2A9
| Solute carrier family 2 (facilitated glucose transporter), member 9
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| Identifiers | ||||||||||||||
| Symbol(s) | SLC2A9; GLUT9; GLUTX | |||||||||||||
| External IDs | OMIM: 606142 MGI: 2152844 Homologene: 69290 | |||||||||||||
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| RNA expression pattern | ||||||||||||||
| Orthologs | ||||||||||||||
| Human | Mouse | |||||||||||||
| Entrez | 56606 | 117591 | ||||||||||||
| Ensembl | ENSG00000109667 | ENSMUSG00000005107 | ||||||||||||
| Uniprot | Q9NRM0 | na | ||||||||||||
| Refseq | NM_001001290 (mRNA) NP_001001290 (protein) |
NM_001012363 (mRNA) NP_001012363 (protein) | ||||||||||||
| Location | Chr 4: 9.44 - 9.65 Mb | Chr 5: 38.64 - 38.79 Mb | ||||||||||||
| Pubmed search | [1] | [2] | ||||||||||||
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [3]
Overview
Solute carrier family 2 (facilitated glucose transporter), member 9, also known as SLC2A9, is a human gene.[1]
This gene encodes a member of the SLC2A facilitative glucose transporter family. Members of this family play a significant role in maintaining glucose homeostasis. The encoded protein may play a role in the development and survival of chondrocytes in cartilage matrices. Two transcript variants encoding distinct isoforms have been identified for this gene.[1]
SLC2A9 has also recently been found to transport uric acid and genetic variants of the transporter have been linked to increased risk of development of gout.[2][3]
See also
References
- ↑ 1.0 1.1 Entrez Gene: SLC2A9 solute carrier family 2 (facilitated glucose transporter), member 9.
- ↑ Vitart V, Rudan I, Hayward C, et al (2008). "SLC2A9 is a newly identified urate transporter influencing serum urate concentration, urate excretion and gout". Nature Genetics 40 (4). doi:10.1038/ng.106.
- ↑ Döring A, Gieger C, Mehta D, et al (2008). "SLC2A9 influences uric acid concentrations with pronounced sex-specific effects". Nature Genetics 40 (4). doi:10.1038/ng.107.
Further reading
- Phay JE, Hussain HB, Moley JF (2000). "Cloning and expression analysis of a novel member of the facilitative glucose transporter family, SLC2A9 (GLUT9).". Genomics 66 (2): 217-20. doi:10.1006/geno.2000.6195. PMID 10860667.
- Doege H, Bocianski A, Joost HG, Schürmann A (2001). "Activity and genomic organization of human glucose transporter 9 (GLUT9), a novel member of the family of sugar-transport facilitators predominantly expressed in brain and leucocytes.". Biochem. J. 350 Pt 3: 771-6. PMID 10970791.
- Shikhman AR, Brinson DC, Valbracht J, Lotz MK (2001). "Cytokine regulation of facilitated glucose transport in human articular chondrocytes.". J. Immunol. 167 (12): 7001-8. PMID 11739520.
- Mobasheri A, Neama G, Bell S, et al. (2002). "Human articular chondrocytes express three facilitative glucose transporter isoforms: GLUT1, GLUT3 and GLUT9.". Cell Biol. Int. 26 (3): 297-300. doi:10.1006/cbir.2001.0850. PMID 11991658.
- 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.
- Richardson S, Neama G, Phillips T, et al. (2003). "Molecular characterization and partial cDNA cloning of facilitative glucose transporters expressed in human articular chondrocytes; stimulation of 2-deoxyglucose uptake by IGF-I and elevated MMP-2 secretion by glucose deprivation.". Osteoarthr. Cartil. 11 (2): 92-101. PMID 12554125.
- 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.
- Augustin R, Carayannopoulos MO, Dowd LO, et al. (2004). "Identification and characterization of human glucose transporter-like protein-9 (GLUT9): alternative splicing alters trafficking.". J. Biol. Chem. 279 (16): 16229-36. doi:10.1074/jbc.M312226200. PMID 14739288.
- 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.
This article incorporates text from the United States National Library of Medicine, which is in the public domain.
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