SLC2A13
SLC2A13 | ||||||
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Identifiers | ||||||
Aliases | SLC2A13, HMIT, solute carrier family 2 member 13 | |||||
External IDs | MGI: 2146030 HomoloGene: 43139 GeneCards: SLC2A13 | |||||
Genetically Related Diseases | ||||||
Parkinson's disease[1] | ||||||
Orthologs | ||||||
Species | Human | Mouse | ||||
Entrez | ||||||
Ensembl | ||||||
UniProt | ||||||
RefSeq (mRNA) | ||||||
RefSeq (protein) | ||||||
Location (UCSC) | Chr 12: 39.76 – 40.11 Mb | Chr 15: 91.27 – 91.57 Mb | ||||
PubMed search | [2] | [3] | ||||
Wikidata |
View/Edit Human | View/Edit Mouse |
Solute carrier family 2 (facilitated glucose transporter), member 13 is a protein that in humans is encoded by the SLC2A13 gene.[4]
References
Further reading
- Uldry, M.; Ibberson, M.; Horisberger, J. D.; Chatton, J. Y.; Riederer, B. M.; Thorens, B. (2001). "Identification of a mammalian H+-myo-inositol symporter expressed predominantly in the brain". The EMBO Journal. 20 (16): 4467–4477. doi:10.1093/emboj/20.16.4467. PMC 125574. PMID 11500374.
- Fu, G. K.; Wang, J. T.; Yang, J.; Au-Young, J.; Stuve, L. L. (2004). "Circular rapid amplification of cDNA ends for high-throughput extension cloning of partial genes". Genomics. 84 (1): 205–210. doi:10.1016/j.ygeno.2004.01.011. PMID 15203218.
- Bankovic, J.; Stojsic, J.; Jovanovic, D.; Andjelkovic, T.; Milinkovic, V.; Ruzdijic, S.; Tanic, N. (2010). "Identification of genes associated with non-small-cell lung cancer promotion and progression". Lung Cancer. 67 (2): 151–159. doi:10.1016/j.lungcan.2009.04.010. PMID 19473719.
- Di Daniel, E.; Mok, M. H.; Mead, E.; Mutinelli, C.; Zambello, E.; Caberlotto, L. L.; Pell, T. J.; Langmead, C. J.; Shah, A. J.; Duddy, G.; Kew, J. N.; Maycox, P. R. (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. (2009). "Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease". Nature Genetics. 41 (12): 1303–1307. doi:10.1038/ng.485. PMID 19915576.
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