Sodium-dependent neutral amino acid transporter B(0)AT1 is a
protein that in humans is encoded by the SLC6A19gene.[5]
Function
SLC6A19 is a system B(0)
transporter that mediates epithelial resorption of neutral amino acids across the
apical membrane in the kidney and intestine.[6][7]
^"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^"Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^
abKleta R, Romeo E, Ristic Z, Ohura T, Stuart C, Arcos-Burgos M, Dave MH, Wagner CA, Camargo SR, Inoue S, Matsuura N, Helip-Wooley A, Bockenhauer D, Warth R, Bernardini I, Visser G, Eggermann T, Lee P, Chairoungdua A, Jutabha P, Babu E, Nilwarangkoon S, Anzai N, Kanai Y, Verrey F, Gahl WA, Koizumi A (September 2004).
"Mutations in SLC6A19, encoding B0AT1, cause Hartnup disorder". Nat. Genet. 36 (9): 999–1002.
doi:10.1038/ng1405.
PMID15286787.
S2CID155361.
Seol SY, Lee SY, Kim YD, et al. (2008). "Minisatellite polymorphisms of the SLC6A19: susceptibility in hypertension". Biochem. Biophys. Res. Commun. 374 (4): 714–719.
doi:
10.1016/j.bbrc.2008.07.094.
PMID18671945.
Mitsuoka K, Shirasaka Y, Fukushi A, et al. (2009). "Transport characteristics of L-citrulline in renal apical membrane of proximal tubular cells". Biopharm Drug Dispos. 30 (3): 126–137.
doi:
10.1002/bdd.653.
PMID19322909.
S2CID20101533.
Azmanov DN, Rodgers H, Auray-Blais C, et al. (2007). "Persistence of the common Hartnup disease D173N allele in populations of European origin". Ann. Hum. Genet. 71 (Pt 6): 755–761.
doi:
10.1111/j.1469-1809.2007.00375.x.
PMID17555458.
S2CID46125073.