solute carrier family 2 (facilitated glucose transporter), member 10 ( - Protein

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Glucose transporter type 10-lacking in arterial tortuosity syndrome-facilitates dehydroascorbic acid transport. [FEBS Lett. 2016]
Glucose transporter type 10-lacking in arterial tortuosity syndrome-facilitates dehydroascorbic acid transport.
Németh CE, Marcolongo P, Gamberucci A, Fulceri R, Benedetti A, Zoppi N, Ritelli M, Chiarelli N, Colombi M, Willaert A, et al. FEBS Lett. 2016 Jun; 590(11):1630-40. Epub 2016 May 27.
GLUT10 deficiency leads to oxidative stress and non-canonical αvβ3 integrin-mediated TGFβ signalling associated with extracellular matrix disarray in arterial tortuosity syndrome skin fibroblasts. [Hum Mol Genet. 2015]
GLUT10 deficiency leads to oxidative stress and non-canonical αvβ3 integrin-mediated TGFβ signalling associated with extracellular matrix disarray in arterial tortuosity syndrome skin fibroblasts.
Zoppi N, Chiarelli N, Cinquina V, Ritelli M, Colombi M. Hum Mol Genet. 2015 Dec 1; 24(23):6769-87. Epub 2015 Sep 16.
Identification of a p.Ser81Arg encoding mutation in SLC2A10 gene of arterial tortuosity syndrome patients from 10 Qatari families. [Clin Genet. 2008]
Identification of a p.Ser81Arg encoding mutation in SLC2A10 gene of arterial tortuosity syndrome patients from 10 Qatari families.
Faiyaz-Ul-Haque M, Zaidi SH, Wahab AA, Eltohami A, Al-Mureikhi MS, Al-Thani G, Peltekova VD, Tsui LC, Teebi AS. Clin Genet. 2008 Aug; 74(2):189-93. Epub 2008 Jun 28.

RefSeq protein
See the reference protein sequence for solute carrier family 2, facilitated glucose transporter member 10 (NP_001102433.1).

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