Sodium-dependent neutral amino acid transporter B
Definition:
References:
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[1]. Robert Kleta, et al. Mutations in SLC6A19, encoding B0AT1, cause Hartnup disorder. Nat Genet. 2004 Sep;36(9):999-1002. [Content Brief]
[2]. Dimitar N Azmanov, et al. Further evidence for allelic heterogeneity in Hartnup disorder. Hum Mutat. 2008 Oct;29(10):1217-21. [Content Brief]
[3]. Sonja Kowalczuk, et al. A protein complex in the brush-border membrane explains a Hartnup disorder allele. FASEB J. 2008 Aug;22(8):2880-7. [Content Brief]
[4]. Heng F Seow, et al. Hartnup disorder is caused by mutations in the gene encoding the neutral amino acid transporter SLC6A19. Nat Genet. 2004 Sep;36(9):1003-7. [Content Brief]
[5]. Simone M R Camargo, et al. Tissue-specific amino acid transporter partners ACE2 and collectrin differentially interact with hartnup mutations. Gastroenterology. 2009 Mar;136(3):872-82. [Content Brief]
[6]. Hitomi Takanaga, et al. Characterization of a branched-chain amino-acid transporter SBAT1 (SLC6A15) that is expressed in human brain. Biochem Biophys Res Commun. 2005 Nov 25;337(3):892-900. [Content Brief]
[7]. Stephen J Fairweather, et al. Molecular basis for the interaction of the mammalian amino acid transporters B0AT1 and B0AT3 with their ancillary protein collectrin. J Biol Chem. 2015 Oct 2;290(40):24308-25. [Content Brief]
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