SLC2A13: Difference between revisions
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'''Solute carrier family 2 (facilitated glucose transporter), member 13''' is a [[protein]] that in humans is encoded by the ''SLC2A13'' [[gene]].<ref name="entrez">{{cite web | title = Entrez Gene: Solute carrier family 2 (facilitated glucose transporter), member 13| url = https://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&cmd=retrieve&list_uids=114134| accessdate = 2011-10-23 <!-- T01:40:44.833-07:00 --> }}</ref> | '''Solute carrier family 2 (facilitated glucose transporter), member 13''' is a [[protein]] that in humans is encoded by the ''SLC2A13'' [[gene]].<ref name="entrez">{{cite web | title = Entrez Gene: Solute carrier family 2 (facilitated glucose transporter), member 13| url = https://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&cmd=retrieve&list_uids=114134| accessdate = 2011-10-23 <!-- T01:40:44.833-07:00 --> }}</ref> | ||
Latest revision as of 18:18, 20 February 2018
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| Location (UCSC) | n/a | n/a | |||||
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Solute carrier family 2 (facilitated glucose transporter), member 13 is a protein that in humans is encoded by the SLC2A13 gene.[1]
References
- ↑ "Entrez Gene: Solute carrier family 2 (facilitated glucose transporter), member 13". Retrieved 2011-10-23.
Further reading
- Uldry M, Ibberson M, Horisberger JD, Chatton JY, Riederer BM, Thorens B (August 2001). "Identification of a mammalian H(+)-myo-inositol symporter expressed predominantly in the brain". The EMBO Journal. 20 (16): 4467–77. doi:10.1093/emboj/20.16.4467. PMC 125574. PMID 11500374.
- Fu GK, Wang JT, Yang J, Au-Young J, Stuve LL (July 2004). "Circular rapid amplification of cDNA ends for high-throughput extension cloning of partial genes". Genomics. 84 (1): 205–10. doi:10.1016/j.ygeno.2004.01.011. PMID 15203218.
- Bankovic J, Stojsic J, Jovanovic D, Andjelkovic T, Milinkovic V, Ruzdijic S, Tanic N (February 2010). "Identification of genes associated with non-small-cell lung cancer promotion and progression". Lung Cancer. 67 (2): 151–9. doi:10.1016/j.lungcan.2009.04.010. PMID 19473719.
- Di Daniel E, Mok MH, Mead E, Mutinelli C, Zambello E, Caberlotto LL, Pell TJ, Langmead CJ, Shah AJ, Duddy G, Kew JN, Maycox PR (July 2009). "Evaluation of expression and function of the H+/myo-inositol transporter HMIT". BMC Cell Biology. 10: 54. doi:10.1186/1471-2121-10-54. PMC 2717050. PMID 19607714.
- Satake W, Nakabayashi Y, Mizuta I, Hirota Y, Ito C, Kubo M, Kawaguchi T, Tsunoda T, Watanabe M, Takeda A, Tomiyama H, Nakashima K, Hasegawa K, Obata F, Yoshikawa T, Kawakami H, Sakoda S, Yamamoto M, Hattori N, Murata M, Nakamura Y, Toda T (December 2009). "Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease". Nature Genetics. 41 (12): 1303–7. doi:10.1038/ng.485. PMID 19915576.
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