Citations for
1FBIS, SLC2A2
Mutations in SLC2A2 gene reveal hGLUT2 function in pancreatic β cell development.
Michau A, Guillemain G, Grosfeld A, Vuillaumier-Barrot S, Grand T, Keck M, L'Hoste S, Chateau D, Serradas P, Teulon J, De Lonlay P, Scharfmann R, Brot-Laroche E, Leturque A, Le Gall M.
J Biol Chem 288(43):31080-92. doi: 10.1074/jbc.M113.469189. Epub 2013 Aug 28. 2013
2FBIS, SLC2A2
Fanconi-Bickel syndrome versus osteogenesis imperfeeta: An Iranian case with a novel mutation in glucose transporter 2 gene, and review of literature.
Hadipour F, Sarkheil P, Noruzinia M, Hadipour Z, Baghdadi T, Shafeghati Y.
Indian J Hum Genet 19(1):84-6. doi: 10.4103/0971-6866.112906. 2013
3SLC2A2
N-Glycosylation modulates the membrane sub-domain distribution and activity of glucose transporter 2 in pancreatic beta cells.
Ohtsubo K, Takamatsu S, Gao C, Korekane H, Kurosawa TM, Taniguchi N.
Biochem Biophys Res Commun 434(2):346-51. doi: 10.1016/j.bbrc.2013.03.076. Epub 2013 Mar 30. 2013
4FBIS, SLC2A2
Fanconi-Bickel syndrome and autosomal recessive proximal tubulopathy with hypercalciuria (ARPTH) are allelic variants caused by GLUT2 mutations.
Mannstadt M, Magen D, Segawa H, Stanley T, Sharma A, Sasaki S, Bergwitz C, Mounien L, Boepple P, Thorens B, Zelikovic I, Jüppner H.
J Clin Endocrinol Metab 97(10):E1978-86. doi: 10.1210/jc.2012-1279. Epub 2012 Aug 3. 2012
5SLC2A2
SLC2A2 mutations can cause neonatal diabetes, suggesting GLUT2 may have a role in human insulin secretion.
Sansbury FH, Flanagan SE, Houghton JA, Shuixian Shen FL, Al-Senani AM, Habeb AM, Abdullah M, Kariminejad A, Ellard S, Hattersley AT.
Diabetologia 55(9):2381-5. doi: 10.1007/s00125-012-2595-0. Epub 2012 Jun 2. 2012
6FBIS, SLC2A2
Fanconi-Bickel syndrome: GLUT2 mutations associated with a mild phenotype.
Grünert SC, Schwab KO, Pohl M, Sass JO, Santer R.
Mol Genet Metab 105(3):433-7. doi: 10.1016/j.ymgme.2011.11.200. Epub 2011 Dec 8. 2012
7SLC2A2
GLUT2 (SLC2A2) is not the principal glucose transporter in human pancreatic beta cells: implications for understanding genetic association signals at this locus.
McCulloch LJ, van de Bunt M, Braun M, Frayn KN, Clark A, Gloyn AL.
Mol Genet Metab 104(4):648-53. doi: 10.1016/j.ymgme.2011.08.026. Epub 2011 Aug 28. 2011
8SLC2A2
The glucose transporter 2 undergoes plasma membrane endocytosis and lysosomal degradation in a secretagogue-dependent manner.
Hou JC, Williams D, Vicogne J, Pessin JE.
Endocrinology 150(9):4056-64. doi: 10.1210/en.2008-1685. Epub 2009 May 28. 2009
9SLC2A2
Loss of sugar detection by GLUT2 affects glucose homeostasis in mice.
Stolarczyk E, Le Gall M, Even P, Houllier A, Serradas P, Brot-Laroche E, Leturque A.
PLoS One 2(12):e1288. 2007
10SLC2A2, MGAT4A
Dietary and genetic control of glucose transporter 2 glycosylation promotes insulin secretion in suppressing diabetes.
Ohtsubo K, Takamatsu S, Minowa MT, Yoshida A, Takeuchi M, Marth JD.
Cell 123(7):1307-21. 2005
11FBIS, SLC2A2
The mutation spectrum of the facilitative glucose transporter gene SLC2A2 (GLUT2) in patients with Fanconi-Bickel syndrome.
Santer R, Groth S, Kinner M, Dombrowski A, Berry GT, Brodehl J, Leonard JV, Moses S, Norgren S, Skovby F, Schneppenheim R, Steinmann B, Schaub J.
Hum Genet 110(1):21-9. 2002
12SLC2A2
GLUT2 is a high affinity glucosamine transporter.
Uldry M, Ibberson M, Hosokawa M, Thorens B.
FEBS Lett 524(1-3):199-203. 2002
13FBIS, SLC2A2
A mutation in GLUT2, not in phosphorylase kinase subunits, in hepato-renal glycogenosis with Fanconi syndrome and low phosphorylase kinase activity.
Burwinkel B, Sanjad SA, Al-Sabban E, Al-Abbad A, Kilimann MW.
Hum Genet 105(3):240-3. 1999
14FBIS, SLC2A2
Mutations in GLUT2, the gene for the liver-type glucose transporter, in patients with Fanconi-Bickel syndrome.
Santer R, Schneppenheim R, Dombrowski A, Gotze H, Steinmann B, Schaub J.
Nat Genet 17(3):324-6. 1997
15SLC2A1, SLC2A2, SLC2A3, SLC2A4, SLC2A5, SLC2A6
Structure, function and biosynthesis of GLUT1.
Mueckler M, Hresko RC, Sato M.
Biochem Soc Trans 25(3):951-4. Review. No abstract available. 1997
16SLC2A2
Mappping the human liver/islet glucose transporter (SLC2A2) gene within a genetic linkage map of chromosome 3q using a (CA)n dinucleotide repeat polymorphism and characterization of the polymorphism in three racial groups.
Matsutani A, et al.
Genomics 13 : 495-501. 1992
17SLC2A2
CA repeat polymorphism in the glucose transporter SLC2A2 gene.
Froguel P, et al.
Nucleic Acids Res 19 : 3754. 1991
18SLC2A2
Dinucleotide repeat polymorphism at the human SLC2A2 locus.
Patel P, et al.
Nucleic Acids Res 19 : 4017. 1991
19SLC2A2
Dinucleotide repeat polymorphism in human SLC2A2/liver facilitative glucose transporter gene on chromosome 3.
Granqvist M, et al.
Nucleic Acids Res 19 : 4791. 1991
20SLC2A2
Racial difference in the allele frequencies of genetic polymorphisms at the SLC2A2 gene locus.
Li SR, et al.
(HGM11) Cytogenet Cell Genet 58 : 1878-1879. 1991
21SLC2A2
Two TaqI RFLPs at the SLC2A2 locus in French caucasian population.
Froguel P, et al.
Nucleic Acids Res 19 : 5799. 1991
22SLC2A2
BgI-I and Kpn-I RFLPs at the human liver/islet glucose transporter (SLC2A2) gene locus.
Li SR, et al.
Nucleic Acids Res 19 : 690. 1991
23SLC2A1, SLC2A2, SLC2A3, SLC2A3P1, SLC2A4, SLC2A5
Facilitative glucose transporters : an expanding family.
Gould GW, et al.
Trends Biochem Sci 15 : 18-23. 1990
24SLC2A2
Polymorphisms of HepG2/erythrocyte glucose-transporter gene. Linkage relationships and implications for genetic analysis of NIDDM.
Kaku K, et al.
Diabetes 39 : 49-56. 1990
25SLC2A1, SLC2A2, SLC2A3, SLC2A3P1, SLC2A4, SLC2A5
Human facilitative glucose transporters. Isolation, functional characterization, and gene localization of cDNAs encoding an isoform (GLUT5) expressed in small intestine, kidney, muscle, and adipose tissue and an unusual glucose transporter pseudogene-like sequence (GLUT6).
Kayano T, et al.
J Biol Chem 265 : 13276-13282. 1990
26SLC2A2
Two EcoRI at the GLUT2 locus.
Patel P, et al.
Nucleic Acids Res 18 : 4956. 1990
27SLC2A2
Two EcoRI RFLPs at the GLUT2 locus.
Vilhelmsdotter S, et al.
Nucleic Acids Res 18 : 6175. 1990
28SLC2A2
Sequence, tissue distribution, and chromosomal localization of mRNA encoding a human glucose transporter-like protein.
Fukumoto H, et al.
Proc Natl Acad Sci U S A 85 : 5434-5438. 1988
29SLC2A2, SLC2A5
Osmotic diarrhoea in genetically transmitted glucose-galactose malabsorption.
Lindqvist B, et al.
Acta Paediatr 52 : 217-219. 1963