Neutral and basic amino acid transport protein rBAT: Difference between revisions

SLC3A1
Identifiers
Aliases	SLC3A1, ATR1, CSNU1, D2H, NBAT, RBAT, solute carrier family 3 member 1
External IDs	OMIM: 104614; MGI: 1195264; HomoloGene: 37289; GeneCards: SLC3A1; OMA:SLC3A1 - orthologs
Gene location (Human)
Chr.	Chromosome 2 (human)
End	44,321,494 bp
Gene location (Mouse)
Chr.	Chromosome 17 (mouse)
End	85,371,664 bp
RNA expression pattern
	Top expressed in
	body of pancreas; ; gallbladder; ; kidney; ; islet of Langerhans; ; rectum; ; oocyte; ; secondary oocyte; ; duodenum; ; right lobe of liver; ; jejunal mucosa;
	Top expressed in
	proximal tubule; ; kidney; ; jejunum; ; ileum; ; proximal straight tubule; ; left lobe of liver; ; intestinal epithelium; ; duodenum; ; intestinal villus; ; coelomic epithelium;
	More reference expression data
	More reference expression data
Gene ontology
Molecular function	amino acid transmembrane transporter activity; basic amino acid transmembrane transporter activity; L-cystine transmembrane transporter activity; catalytic activity; protein binding; protein heterodimerization activity;
Cellular component	integral component of membrane; membrane; vacuolar membrane; plasma membrane; integral component of plasma membrane; brush border membrane; mitochondrial inner membrane; extracellular exosome;
Biological process	cellular amino acid metabolic process; basic amino acid transport; amino acid transport; L-cystine transport; amino acid transmembrane transport; basic amino acid transmembrane transport; transport; carbohydrate metabolic process;
	Sources:Amigo / QuickGO
Orthologs
	6519
	20532
	ENSG00000138079
	ENSMUSG00000024131
	Q07837
	Q91WV7
	NM_000341
	NM_009205
	NP_000332
	NP_033231
	Wikidata
View/Edit Human	View/Edit Mouse

Browse history interactively

← Previous edit

Content deleted Content added

VisualWikitext

Inline

Latest revision as of 12:56, 4 January 2024

Neutral and basic amino acid transport protein rBAT is a protein that in humans is encoded by the SLC3A1 gene.^[5]^[6]^[7]

Mutations in the SLC3A1 gene are associated with cystinuria.

References[edit]

^ ^a ^b ^c GRCh38: Ensembl release 89: ENSG00000138079 – Ensembl, May 2017
^ ^a ^b ^c GRCm38: Ensembl release 89: ENSMUSG00000024131 – Ensembl, May 2017
^ "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.
^ Lee WS, Wells RG, Sabbag RV, Mohandas TK, Hediger MA (Jun 1993). "Cloning and chromosomal localization of a human kidney cDNA involved in cystine, dibasic, and neutral amino acid transport". J Clin Invest. 91 (5): 1959–1963. doi:10.1172/JCI116415. PMC 288191. PMID 8486766.
^ Endsley JK, Phillips JA, Hruska KA, Denneberg T, Carlson J, George AL (Aug 1997). "Genomic organization of a human cystine transporter gene (SLC3A1) and identification of novel mutations causing cystinuria". Kidney Int. 51 (6): 1893–1899. doi:10.1038/ki.1997.258. PMID 9186880.
^ "Entrez Gene: SLC3A1 solute carrier family 3 (cystine, dibasic and neutral amino acid transporters, activator of cystine, dibasic and neutral amino acid transport), member 1".

Further reading[edit]

Pras E, Raben N, Golomb E, Arber N, Aksentijevich I, Schapiro JM, Harel D, Katz G, Liberman U, Pras M (1995). "Mutations in the SLC3A1 transporter gene in cystinuria". Am. J. Hum. Genet. 56 (6): 1297–303. PMC 1801089. PMID 7539209.
Calonge MJ, Volpini V, Bisceglia L, Rousaud F, de Sanctis L, Beccia E, Zelante L, Testar X, Zorzano A, Estivill X (1995). "Genetic heterogeneity in cystinuria: the SLC3A1 gene is linked to type I but not to type III cystinuria". Proc. Natl. Acad. Sci. U.S.A. 92 (21): 9667–9671. Bibcode:1995PNAS...92.9667C. doi:10.1073/pnas.92.21.9667. PMC 40863. PMID 7568194.
Gasparini P, Calonge MJ, Bisceglia L, Purroy J, Dianzani I, Notarangelo A, Rousaud F, Gallucci M, Testar X, Ponzone A (1995). "Molecular genetics of cystinuria: identification of four new mutations and seven polymorphisms, and evidence for genetic heterogeneity". Am. J. Hum. Genet. 57 (4): 781–8. PMC 1801520. PMID 7573036.
Miyamoto K, Katai K, Tatsumi S, Sone K, Segawa H, Yamamoto H, Taketani Y, Takada K, Morita K, Kanayama H (1995). "Mutations of the basic amino acid transporter gene associated with cystinuria". Biochem. J. 310 (3): 951–5. doi:10.1042/bj3100951. PMC 1135988. PMID 7575432.
Bertran J, Werner A, Chillarón J, Nunes V, Biber J, Testar X, Zorzano A, Estivill X, Murer H, Palacín M (1993). "Expression cloning of a human renal cDNA that induces high affinity transport of L-cystine shared with dibasic amino acids in Xenopus oocytes". J. Biol. Chem. 268 (20): 14842–9. doi:10.1016/S0021-9258(18)82410-3. hdl:2445/181367. PMID 7686906.
Busch AE, Herzer T, Waldegger S, Schmidt F, Palacin M, Biber J, et al. (1994). "Opposite directed currents induced by the transport of dibasic and neutral amino acids in Xenopus oocytes expressing the protein rBAT". J. Biol. Chem. 269 (41): 25581–6. doi:10.1016/S0021-9258(18)47289-4. PMID 7929260.
Calonge MJ, Nadal M, Calvano S, Testar X, Zelante L, Zorzano A, Estivill X, Gasparini P, Palacín M, Nunes V (1995). "Assignment of the gene responsible for cystinuria (rBAT) and of markers D2S119 and D2S177 to 2p16 by fluorescence in situ hybridization". Hum. Genet. 95 (6): 633–6. doi:10.1007/bf00209478. PMID 7789946. S2CID 60440459.
Calonge MJ, Gasparini P, Chillarón J, Chillón M, Gallucci M, Rousaud F, Zelante L, Testar X, Dallapiccola B, Di Silverio F (1994). "Cystinuria caused by mutations in rBAT, a gene involved in the transport of cystine". Nat. Genet. 6 (4): 420–425. doi:10.1038/ng0494-420. PMID 8054986. S2CID 6627286.
Ahmed A, Peter GJ, Taylor PM, Harper AA, Rennie MJ (1995). "Sodium-independent Currents of Opposite Polarity Evoked by Neutral and Cationic Amino Acids in Neutral and Basic Amino Acid Transporter cRNA-injected Oocytes". J. Biol. Chem. 270 (21): 8482–8486. doi:10.1074/jbc.270.15.8482. PMID 7721744.
Maruyama K, Sugano S (1994). "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides". Gene. 138 (1–2): 171–174. doi:10.1016/0378-1119(94)90802-8. PMID 8125298.
Miyamoto K, Segawa H, Tatsumi S, Katai K, Yamamoto H, Taketani Y, Haga H, Morita K, Takeda E (1996). "Effects of truncation of the COOH-terminal region of a Na+-independent neutral and basic amino acid transporter on amino acid transport in Xenopus oocytes". J. Biol. Chem. 271 (28): 16758–16763. doi:10.1074/jbc.271.28.16758. PMID 8663184.
Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, Suyama A, Sugano S (1997). "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library". Gene. 200 (1–2): 149–156. doi:10.1016/S0378-1119(97)00411-3. PMID 9373149.
Ahmed A, Yao PC, Brant AM, Peter GJ, Harper AA (1997). "Electrogenic L-Histidine Transport in Neutral and Basic Amino Acid Transporter (NBAT)-expressing Xenopus laevis Oocytes". J. Biol. Chem. 272 (1): 125–130. doi:10.1074/jbc.272.1.125. PMID 8995237.
Rossier G, Meier C, Bauch C, Summa V, Sordat B, Verrey F, Kühn LC (2000). "LAT2, a new basolateral 4F2hc/CD98-associated amino acid transporter of kidney and intestine". J. Biol. Chem. 274 (49): 34948–34954. doi:10.1074/jbc.274.49.34948. PMID 10574970.
Pfeiffer R, Loffing J, Rossier G, Bauch C, Meier C, Eggermann T, Loffing-Cueni D, Kühn LC, Verrey F (2000). "Luminal heterodimeric amino acid transporter defective in cystinuria". Mol. Biol. Cell. 10 (12): 4135–47. doi:10.1091/mbc.10.12.4135. PMC 25748. PMID 10588648.
Rajan DP, Huang W, Kekuda R, George RL, Wang J, Conway SJ, Devoe LD, Leibach FH, Prasad PD, Ganapathy V (2000). "Differential influence of the 4F2 heavy chain and the protein related to b(0,+) amino acid transport on substrate affinity of the heteromeric b(0,+) amino acid transporter". J. Biol. Chem. 275 (19): 14331–14335. doi:10.1074/jbc.275.19.14331. PMID 10799513.
Mizoguchi K, Cha SH, Chairoungdua A, Kim DK, Shigeta Y, Matsuo H, Fukushima J, Awa Y, Akakura K, Goya T, Ito H, Endou H, Kanai Y (2001). "Human cystinuria-related transporter: localization and functional characterization". Kidney Int. 59 (5): 1821–1833. doi:10.1046/j.1523-1755.2001.0590051821.x. PMID 11318953.
Harnevik L, Fjellstedt E, Molbaek A, Tiselius HG, Denneberg T, Söderkvist P (2002). "Identification of 12 novel mutations in the SLC3A1 gene in Swedish cystinuria patients". Hum. Mutat. 18 (6): 516–525. doi:10.1002/humu.1228. PMID 11748844. S2CID 30914353.
Bauch C, Verrey F (2002). "Apical heterodimeric cystine and cationic amino acid transporter expressed in MDCK cells". Am. J. Physiol. Renal Physiol. 283 (1): F181–9. doi:10.1152/ajprenal.00212.2001. PMID 12060600. S2CID 20811615.
Fernández E, Carrascal M, Rousaud F, Abián J, Zorzano A, Palacín M, Chillarón J (2002). "rBAT-b(0,+)AT heterodimer is the main apical reabsorption system for cystine in the kidney". Am. J. Physiol. Renal Physiol. 283 (3): F540–8. doi:10.1152/ajprenal.00071.2002. PMID 12167606.
Botzenhart E, Vester U, Schmidt C, Hesse A, Halber M, Wagner C, Lang F, Hoyer P, Zerres K, Eggermann T (2003). "Cystinuria in children: distribution and frequencies of mutations in the SLC3A1 and SLC7A9 genes". Kidney Int. 62 (4): 1136–1142. doi:10.1111/j.1523-1755.2002.kid552.x. PMID 12234283.

This membrane protein–related article is a stub. You can help Wikipedia by expanding it.

[refGRCh38Ensembl-1] GRCh38: Ensembl release 89: ENSG00000138079 – Ensembl, May 2017

[refGRCm38Ensembl-2] GRCm38: Ensembl release 89: ENSMUSG00000024131 – Ensembl, May 2017

[3] "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[4] "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[pmid8486766-5] Lee WS, Wells RG, Sabbag RV, Mohandas TK, Hediger MA (Jun 1993). "Cloning and chromosomal localization of a human kidney cDNA involved in cystine, dibasic, and neutral amino acid transport". J Clin Invest. 91 (5): 1959–1963. doi:10.1172/JCI116415. PMC 288191. PMID 8486766.

[pmid9186880-6] Endsley JK, Phillips JA, Hruska KA, Denneberg T, Carlson J, George AL (Aug 1997). "Genomic organization of a human cystine transporter gene (SLC3A1) and identification of novel mutations causing cystinuria". Kidney Int. 51 (6): 1893–1899. doi:10.1038/ki.1997.258. PMID 9186880.

[entrez-7] "Entrez Gene: SLC3A1 solute carrier family 3 (cystine, dibasic and neutral amino acid transporters, activator of cystine, dibasic and neutral amino acid transport), member 1".

[1]

[2]

[3]

[4]

[5]

[6]

[7]

@@ Line 1: / Line 1: @@
+{{Short description|Protein-coding gene in the species Homo sapiens}}
-{{PBB|geneid=6519}}
+{{Infobox_gene}}
-'''Neutral and basic amino acid transport protein rBAT''' is a [[protein]] that in humans is encoded by the ''SLC3A1'' [[gene]].<ref name="pmid8486766">{{cite journal | author = Lee WS, Wells RG, Sabbag RV, Mohandas TK, Hediger MA | title = Cloning and chromosomal localization of a human kidney cDNA involved in cystine, dibasic, and neutral amino acid transport | journal = J Clin Invest | volume = 91 | issue = 5 | pages = 1959–1963 |date=Jun 1993 | pmid = 8486766 | pmc = 288191 | doi = 10.1172/JCI116415 }}</ref><ref name="pmid9186880">{{cite journal | author = Endsley JK, Phillips JA 3rd, Hruska KA, Denneberg T, Carlson J, George AL Jr | title = Genomic organization of a human cystine transporter gene (SLC3A1) and identification of novel mutations causing cystinuria | journal = Kidney Int | volume = 51 | issue = 6 | pages = 1893–1899 |date=Aug 1997 | pmid = 9186880 | pmc =  | doi =10.1038/ki.1997.258  }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: SLC3A1 solute carrier family 3 (cystine, dibasic and neutral amino acid transporters, activator of cystine, dibasic and neutral amino acid transport), member 1| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=6519| accessdate = }}</ref>
+'''Neutral and basic amino acid transport protein rBAT''' is a [[protein]] that in humans is encoded by the ''SLC3A1'' [[gene]].<ref name="pmid8486766">{{cite journal | vauthors = Lee WS, Wells RG, Sabbag RV, Mohandas TK, Hediger MA | title = Cloning and chromosomal localization of a human kidney cDNA involved in cystine, dibasic, and neutral amino acid transport | journal = J Clin Invest | volume = 91 | issue = 5 | pages = 1959–1963 | date = Jun 1993 | pmid = 8486766 | pmc = 288191 | doi = 10.1172/JCI116415 }}</ref><ref name="pmid9186880">{{cite journal | vauthors = Endsley JK, Phillips JA, Hruska KA, Denneberg T, Carlson J, George AL | title = Genomic organization of a human cystine transporter gene (SLC3A1) and identification of novel mutations causing cystinuria | journal = Kidney Int | volume = 51 | issue = 6 | pages = 1893–1899 | date = Aug 1997 | pmid = 9186880 | doi = 10.1038/ki.1997.258 | doi-access = free }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: SLC3A1 solute carrier family 3 (cystine, dibasic and neutral amino acid transporters, activator of cystine, dibasic and neutral amino acid transport), member 1| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=6519}}</ref>
 Mutations in the SLC3A1 gene are associated with [[cystinuria]].
-==See also==
+== See also ==
 * [[Heterodimeric amino acid transporter]]
 * [[Solute carrier family]]
-==References==
+== References ==
 {{reflist}}
-==Further reading==
+== Further reading ==
 {{refbegin | 2}}
+* {{cite journal | vauthors = Pras E, Raben N, Golomb E, Arber N, Aksentijevich I, Schapiro JM, Harel D, Katz G, Liberman U, Pras M | title = Mutations in the SLC3A1 transporter gene in cystinuria | journal = Am. J. Hum. Genet. | volume = 56 | issue = 6 | pages = 1297–303 | year = 1995 | pmid = 7539209 | pmc = 1801089 }}
-*{{cite journal  | author=Pras E |title=Mutations in the SLC3A1 transporter gene in cystinuria |journal=Am. J. Hum. Genet. |volume=56 |issue= 6 |pages= 1297–303 |year= 1995 |pmid= 7539209 |doi=  | pmc=1801089  | author-separator=,  | author2=Raben N  | author3=Golomb E  | display-authors=3  | last4=Arber  | first4=N  | last5=Aksentijevich  | first5=I  | last6=Schapiro  | first6=JM  | last7=Harel  | first7=D  | last8=Katz  | first8=G  | last9=Liberman  | first9=U  }}
-*{{cite journal  | author=Calonge MJ |title=Genetic heterogeneity in cystinuria: the SLC3A1 gene is linked to type I but not to type III cystinuria |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=92 |issue= 21 |pages= 9667–9671 |year= 1995 |pmid= 7568194 |doi=10.1073/pnas.92.21.9667  | pmc=40863  | author-separator=,  | author2=Volpini V  | author3=Bisceglia L  | display-authors=3  | last4=Rousaud  | first4=F  | last5=De Sanctis  | first5=L  | last6=Beccia  | first6=E  | last7=Zelante  | first7=L  | last8=Testar  | first8=X  | last9=Zorzano  | first9=A  }}
+* {{cite journal | vauthors = Calonge MJ, Volpini V, Bisceglia L, Rousaud F, de Sanctis L, Beccia E, Zelante L, Testar X, Zorzano A, Estivill X | title = Genetic heterogeneity in cystinuria: the SLC3A1 gene is linked to type I but not to type III cystinuria | journal = Proc. Natl. Acad. Sci. U.S.A. | volume = 92 | issue = 21 | pages = 9667–9671 | year = 1995 | pmid = 7568194 | pmc = 40863 | doi = 10.1073/pnas.92.21.9667 | bibcode = 1995PNAS...92.9667C | doi-access = free }}
-*{{cite journal  | author=Gasparini P |title=Molecular genetics of cystinuria: identification of four new mutations and seven polymorphisms, and evidence for genetic heterogeneity |journal=Am. J. Hum. Genet. |volume=57 |issue= 4 |pages= 781–8 |year= 1995 |pmid= 7573036 |doi=  | pmc=1801520  | author-separator=,  | author2=Calonge MJ  | author3=Bisceglia L  | display-authors=3  | last4=Purroy  | first4=J  | last5=Dianzani  | first5=I  | last6=Notarangelo  | first6=A  | last7=Rousaud  | first7=F  | last8=Gallucci  | first8=M  | last9=Testar  | first9=X  }}
+* {{cite journal | vauthors = Gasparini P, Calonge MJ, Bisceglia L, Purroy J, Dianzani I, Notarangelo A, Rousaud F, Gallucci M, Testar X, Ponzone A | title = Molecular genetics of cystinuria: identification of four new mutations and seven polymorphisms, and evidence for genetic heterogeneity | journal = Am. J. Hum. Genet. | volume = 57 | issue = 4 | pages = 781–8 | year = 1995 | pmid = 7573036 | pmc = 1801520 }}
+* {{cite journal | vauthors = Miyamoto K, Katai K, Tatsumi S, Sone K, Segawa H, Yamamoto H, Taketani Y, Takada K, Morita K, Kanayama H | title = Mutations of the basic amino acid transporter gene associated with cystinuria | journal = Biochem. J. | volume = 310 | issue = 3 | pages = 951–5 | year = 1995 | pmid = 7575432 | pmc = 1135988 | doi =  10.1042/bj3100951}}
-*{{cite journal  | author=Miyamoto K |title=Mutations of the basic amino acid transporter gene associated with cystinuria |journal=Biochem. J. |volume=310 |issue=  3|pages= 951–5 |year= 1995 |pmid= 7575432 |doi=  | pmc=1135988  | author-separator=,  | author2=Katai K  | author3=Tatsumi S  | display-authors=3  | last4=Sone  | first4=K  | last5=Segawa  | first5=H  | last6=Yamamoto  | first6=H  | last7=Taketani  | first7=Y  | last8=Takada  | first8=K  | last9=Morita  | first9=K  }}
-*{{cite journal  | author=Bertran J |title=Expression cloning of a human renal cDNA that induces high affinity transport of L-cystine shared with dibasic amino acids in Xenopus oocytes |journal=J. Biol. Chem. |volume=268 |issue= 20 |pages= 14842–9 |year= 1993 |pmid= 7686906 |doi=  | author-separator=,  | author2=Werner A  | author3=Chillarón J  | display-authors=3  | last4=Nunes  | first4=V  | last5=Biber  | first5=J  | last6=Testar  | first6=X  | last7=Zorzano  | first7=A  | last8=Estivill  | first8=X  | last9=Murer  | first9=H  }}
+* {{cite journal | vauthors = Bertran J, Werner A, Chillarón J, Nunes V, Biber J, Testar X, Zorzano A, Estivill X, Murer H, Palacín M | title = Expression cloning of a human renal cDNA that induces high affinity transport of L-cystine shared with dibasic amino acids in Xenopus oocytes | journal = J. Biol. Chem. | volume = 268 | issue = 20 | pages = 14842–9 | year = 1993 | doi = 10.1016/S0021-9258(18)82410-3 | pmid = 7686906 | doi-access = free | hdl = 2445/181367 | hdl-access = free }}
-*{{cite journal  | author= Busch|title= Opposite directed currents induced by the transport of dibasic and neutral amino acids in Xenopus oocytes expressing the protein rBAT |journal= J. Biol. Chem.  | volume= 269 |pages= 25581–6 |year= 1994  |pmid= 7929260  | issue= 41  | author-separator= ,  | author2= A  | author3= Herzer  | author4= T  | author5= Waldegger  | author6= S  | display-authors= 6  | last7= Markovich  | first7= D  | last8= Murer  | first8= H  | last9= Lang  | first9= F }}
+* {{cite journal | vauthors = Busch AE, Herzer T, Waldegger S, Schmidt F, Palacin M, Biber J, Markovich D, Murer H, Lang F | title = Opposite directed currents induced by the transport of dibasic and neutral amino acids in Xenopus oocytes expressing the protein rBAT | journal = J. Biol. Chem. | volume = 269 | issue = 41 | pages = 25581–6 | year = 1994 | pmid = 7929260 | last8 = Murer | first8 = H | last9 = Lang | display-authors = 6 | first9 = F | last7 = Markovich | first7 = D | doi = 10.1016/S0021-9258(18)47289-4 | doi-access = free }}
-*{{cite journal  | author=Calonge MJ |title=Assignment of the gene responsible for cystinuria (rBAT) and of markers D2S119 and D2S177 to 2p16 by fluorescence in situ hybridization |journal=Hum. Genet. |volume=95 |issue= 6 |pages= 633–6 |year= 1995 |pmid= 7789946 |doi=  10.1007/bf00209478| author-separator=,  | author2=Nadal M  | author3=Calvano S  | display-authors=3  | last4=Testar  | first4=X  | last5=Zelante  | first5=L  | last6=Zorzano  | first6=A  | last7=Estivill  | first7=X  | last8=Gasparini  | first8=P  | last9=Palacín  | first9=M  }}
+* {{cite journal | vauthors = Calonge MJ, Nadal M, Calvano S, Testar X, Zelante L, Zorzano A, Estivill X, Gasparini P, Palacín M, Nunes V | title = Assignment of the gene responsible for cystinuria (rBAT) and of markers D2S119 and D2S177 to 2p16 by fluorescence in situ hybridization | journal = Hum. Genet. | volume = 95 | issue = 6 | pages = 633–6 | year = 1995 | pmid = 7789946 | doi = 10.1007/bf00209478 | s2cid = 60440459 }}
-*{{cite journal  | author=Calonge MJ |title=Cystinuria caused by mutations in rBAT, a gene involved in the transport of cystine |journal=Nat. Genet. |volume=6 |issue= 4 |pages= 420–425 |year= 1994 |pmid= 8054986 |doi= 10.1038/ng0494-420  | author-separator=,  | author2=Gasparini P  | author3=Chillarón J  | display-authors=3  | last4=Chillón  | first4=Miguel  | last5=Gallucci  | first5=Michele  | last6=Rousaud  | first6=Ferran  | last7=Zelante  | first7=Leopoldo  | last8=Testar  | first8=Xavier  | last9=Dallapiccola  | first9=Bruno }}
+* {{cite journal | vauthors = Calonge MJ, Gasparini P, Chillarón J, Chillón M, Gallucci M, Rousaud F, Zelante L, Testar X, Dallapiccola B, Di Silverio F | title = Cystinuria caused by mutations in rBAT, a gene involved in the transport of cystine | journal = Nat. Genet. | volume = 6 | issue = 4 | pages = 420–425 | year = 1994 | pmid = 8054986 | doi = 10.1038/ng0494-420 | s2cid = 6627286 }}
-*{{cite journal  | author= Ahmed|title= Sodium-independent Currents of Opposite Polarity Evoked by Neutral and Cationic Amino Acids in Neutral and Basic Amino Acid Transporter cRNA-injected Oocytes |journal= J. Biol. Chem.  | volume=270 |pages= 8482–8486 |year= 1995 |pmid= 7721744 |doi= 10.1074/jbc.270.15.8482  | issue= 21  | pmc=  | author-separator= ,  | author2= A  | author3= Peter  | author4= G  | author5= Taylor  | author6= P  | display-authors= 6 }}
+* {{cite journal | vauthors = Ahmed A, Peter GJ, Taylor PM, Harper AA, Rennie MJ | title = Sodium-independent Currents of Opposite Polarity Evoked by Neutral and Cationic Amino Acids in Neutral and Basic Amino Acid Transporter cRNA-injected Oocytes | journal = J. Biol. Chem. | volume = 270 | issue = 21 | pages = 8482–8486 | year = 1995 | pmid = 7721744 | doi = 10.1074/jbc.270.15.8482 | doi-access = free }}
-*{{cite journal  | author=Maruyama K, Sugano S |title=Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides |journal=Gene |volume=138 |issue= 1–2 |pages= 171–174 |year= 1994 |pmid= 8125298 |doi=10.1016/0378-1119(94)90802-8  }}
+* {{cite journal | vauthors = Maruyama K, Sugano S | title = Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides | journal = Gene | volume = 138 | issue = 1–2 | pages = 171–174 | year = 1994 | pmid = 8125298 | doi = 10.1016/0378-1119(94)90802-8 }}
-*{{cite journal  | author=Miyamoto K |title=Effects of truncation of the COOH-terminal region of a Na+-independent neutral and basic amino acid transporter on amino acid transport in Xenopus oocytes |journal=J. Biol. Chem. |volume=271 |issue= 28 |pages= 16758–16763 |year= 1996 |pmid= 8663184 |doi=10.1074/jbc.271.28.16758  | author-separator=,  | author2=Segawa H  | author3=Tatsumi S  | display-authors=3  | last4=Katai  | first4=K  | last5=Yamamoto  | first5=H  | last6=Taketani  | first6=Y  | last7=Haga  | first7=H  | last8=Morita  | first8=K  | last9=Takeda  | first9=E  }}
+* {{cite journal | vauthors = Miyamoto K, Segawa H, Tatsumi S, Katai K, Yamamoto H, Taketani Y, Haga H, Morita K, Takeda E | title = Effects of truncation of the COOH-terminal region of a Na+-independent neutral and basic amino acid transporter on amino acid transport in Xenopus oocytes | journal = J. Biol. Chem. | volume = 271 | issue = 28 | pages = 16758–16763 | year = 1996 | pmid = 8663184 | doi = 10.1074/jbc.271.28.16758 | doi-access = free }}
-*{{cite journal  | author=Suzuki Y |title=Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library |journal=Gene |volume=200 |issue= 1–2 |pages= 149–156 |year= 1997 |pmid= 9373149 |doi=10.1016/S0378-1119(97)00411-3  | author-separator=,  | author2=Yoshitomo-Nakagawa K  | author3=Maruyama K  | display-authors=3  | last4=Suyama  | first4=A  | last5=Sugano  | first5=S  }}
+* {{cite journal | vauthors = Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, Suyama A, Sugano S | title = Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library | journal = Gene | volume = 200 | issue = 1–2 | pages = 149–156 | year = 1997 | pmid = 9373149 | doi = 10.1016/S0378-1119(97)00411-3 }}
-*{{cite journal  | author= Ahmed|title= Electrogenic L-Histidine Transport in Neutral and Basic Amino Acid Transporter (NBAT)-expressing Xenopus laevis Oocytes |journal= J. Biol. Chem.  | volume= 272 |pages= 125–130 |year= 1997 |pmid= 8995237 |doi= 10.1074/jbc.272.1.125  | issue= 1  | author-separator= ,  | author2= A  | author3= Yao  | author4= P  | author5= Brant  | author6= A  | display-authors= 6}}
+* {{cite journal | vauthors = Ahmed A, Yao PC, Brant AM, Peter GJ, Harper AA | title = Electrogenic L-Histidine Transport in Neutral and Basic Amino Acid Transporter (NBAT)-expressing Xenopus laevis Oocytes | journal = J. Biol. Chem. | volume = 272 | issue = 1 | pages = 125–130 | year = 1997 | pmid = 8995237 | doi = 10.1074/jbc.272.1.125 | doi-access = free }}
-*{{cite journal  | author=Rossier G |title=LAT2, a new basolateral 4F2hc/CD98-associated amino acid transporter of kidney and intestine |journal=J. Biol. Chem. |volume=274 |issue= 49 |pages= 34948–34954 |year= 2000 |pmid= 10574970 |doi=10.1074/jbc.274.49.34948  | author-separator=,  | author2=Meier C  | author3=Bauch C  | display-authors=3  | last4=Summa  | first4=V  | last5=Sordat  | first5=B  | last6=Verrey  | first6=F  | last7=Kühn  | first7=LC  }}
+* {{cite journal | vauthors = Rossier G, Meier C, Bauch C, Summa V, Sordat B, Verrey F, Kühn LC | title = LAT2, a new basolateral 4F2hc/CD98-associated amino acid transporter of kidney and intestine | journal = J. Biol. Chem. | volume = 274 | issue = 49 | pages = 34948–34954 | year = 2000 | pmid = 10574970 | doi = 10.1074/jbc.274.49.34948 | doi-access = free }}
+* {{cite journal | vauthors = Pfeiffer R, Loffing J, Rossier G, Bauch C, Meier C, Eggermann T, Loffing-Cueni D, Kühn LC, Verrey F | title = Luminal heterodimeric amino acid transporter defective in cystinuria | journal = Mol. Biol. Cell | volume = 10 | issue = 12 | pages = 4135–47 | year = 2000 | pmid = 10588648 | pmc = 25748 | doi = 10.1091/mbc.10.12.4135 }}
-*{{cite journal  | author=Pfeiffer R |title=Luminal heterodimeric amino acid transporter defective in cystinuria |journal=Mol. Biol. Cell |volume=10 |issue= 12 |pages= 4135–47 |year= 2000 |pmid= 10588648 |doi=  | pmc=25748  | author-separator=,  | author2=Loffing J  | author3=Rossier G  | display-authors=3  | last4=Bauch  | first4=C  | last5=Meier  | first5=C  | last6=Eggermann  | first6=T  | last7=Loffing-Cueni  | first7=D  | last8=Kühn  | first8=LC  | last9=Verrey  | first9=F  }}
-*{{cite journal  | author=Rajan DP |title=Differential influence of the 4F2 heavy chain and the protein related to b(0,+) amino acid transport on substrate affinity of the heteromeric b(0,+) amino acid transporter |journal=J. Biol. Chem. |volume=275 |issue= 19 |pages= 14331–14335 |year= 2000 |pmid= 10799513 |doi=10.1074/jbc.275.19.14331  | author-separator=,  | author2=Huang W  | author3=Kekuda R  | display-authors=3  | last4=George  | first4=RL  | last5=Wang  | first5=J  | last6=Conway  | first6=SJ  | last7=Devoe  | first7=LD  | last8=Leibach  | first8=FH  | last9=Prasad  | first9=PD  }}
+* {{cite journal | vauthors = Rajan DP, Huang W, Kekuda R, George RL, Wang J, Conway SJ, Devoe LD, Leibach FH, Prasad PD, Ganapathy V | title = Differential influence of the 4F2 heavy chain and the protein related to b(0,+) amino acid transport on substrate affinity of the heteromeric b(0,+) amino acid transporter | journal = J. Biol. Chem. | volume = 275 | issue = 19 | pages = 14331–14335 | year = 2000 | pmid = 10799513 | doi = 10.1074/jbc.275.19.14331 | doi-access = free }}
-*{{cite journal  | author=Mizoguchi K |title=Human cystinuria-related transporter: localization and functional characterization |journal=Kidney Int. |volume=59 |issue= 5 |pages= 1821–1833 |year= 2001 |pmid= 11318953 |doi= 10.1046/j.1523-1755.2001.0590051821.x  | author-separator=,  | author2=Cha SH  | author3=Chairoungdua A  | display-authors=3  | last4=Kim  | first4=Do Kyung  | last5=Shigeta  | first5=Yasuhiro  | last6=Matsuo  | first6=Hirotaka  | last7=Fukushima  | first7=Jun-Ichi  | last8=Awa  | first8=Yusuke  | last9=Akakura  | first9=Koichiro }}
+* {{cite journal | vauthors = Mizoguchi K, Cha SH, Chairoungdua A, Kim DK, Shigeta Y, Matsuo H, Fukushima J, Awa Y, Akakura K, Goya T, Ito H, Endou H, Kanai Y | title = Human cystinuria-related transporter: localization and functional characterization | journal = Kidney Int. | volume = 59 | issue = 5 | pages = 1821–1833 | year = 2001 | pmid = 11318953 | doi = 10.1046/j.1523-1755.2001.0590051821.x | doi-access = free }}
-*{{cite journal  | author=Harnevik L |title=Identification of 12 novel mutations in the SLC3A1 gene in Swedish cystinuria patients |journal=Hum. Mutat. |volume=18 |issue= 6 |pages= 516–525 |year= 2002 |pmid= 11748844 |doi= 10.1002/humu.1228  | author-separator=,  | author2=Fjellstedt E  | author3=Molbaek A  | display-authors=3  | last4=Tiselius  | first4=Hans-G�ran  | last5=Denneberg  | first5=Torsten  | last6=s�Derkvist  | first6=Peter }}
+* {{cite journal | vauthors = Harnevik L, Fjellstedt E, Molbaek A, Tiselius HG, Denneberg T, Söderkvist P | title = Identification of 12 novel mutations in the SLC3A1 gene in Swedish cystinuria patients | journal = Hum. Mutat. | volume = 18 | issue = 6 | pages = 516–525 | year = 2002 | pmid = 11748844 | doi = 10.1002/humu.1228 | s2cid = 30914353 }}
-*{{cite journal  | author=Bauch C, Verrey F |title=Apical heterodimeric cystine and cationic amino acid transporter expressed in MDCK cells |journal=Am. J. Physiol. Renal Physiol. |volume=283 |issue= 1 |pages= F181–9 |year= 2002 |pmid= 12060600 |doi= 10.1152/ajprenal.00212.2001 }}
+* {{cite journal | vauthors = Bauch C, Verrey F | title = Apical heterodimeric cystine and cationic amino acid transporter expressed in MDCK cells | journal = Am. J. Physiol. Renal Physiol. | volume = 283 | issue = 1 | pages = F181–9 | year = 2002 | pmid = 12060600 | doi = 10.1152/ajprenal.00212.2001 | s2cid = 20811615 }}
-*{{cite journal  | author=Fernández E |title=rBAT-b(0,+)AT heterodimer is the main apical reabsorption system for cystine in the kidney |journal=Am. J. Physiol. Renal Physiol. |volume=283 |issue= 3 |pages= F540–8 |year= 2002 |pmid= 12167606 |doi= 10.1152/ajprenal.00071.2002  | author-separator=,  | author2=Carrascal M  | author3=Rousaud F  | display-authors=3  | last4=Abián  | first4=J  | last5=Zorzano  | first5=A  | last6=Palacín  | first6=M  | last7=Chillarón  | first7=J }}
+* {{cite journal | vauthors = Fernández E, Carrascal M, Rousaud F, Abián J, Zorzano A, Palacín M, Chillarón J | title = rBAT-b(0,+)AT heterodimer is the main apical reabsorption system for cystine in the kidney | journal = Am. J. Physiol. Renal Physiol. | volume = 283 | issue = 3 | pages = F540–8 | year = 2002 | pmid = 12167606 | doi = 10.1152/ajprenal.00071.2002 }}
-*{{cite journal  | author=Botzenhart E |title=Cystinuria in children: distribution and frequencies of mutations in the SLC3A1 and SLC7A9 genes |journal=Kidney Int. |volume=62 |issue= 4 |pages= 1136–1142 |year= 2003 |pmid= 12234283 |doi= 10.1111/j.1523-1755.2002.kid552.x  | author-separator=,  | author2=Vester U  | author3=Schmidt C  | display-authors=3  | last4=Hesse  | first4=Albrecht  | last5=Halber  | first5=Marc  | last6=Wagner  | first6=Carsten  | last7=Lang  | first7=Florian  | last8=Hoyer  | first8=Peter  | last9=Zerres  | first9=Klaus }}
+* {{cite journal | vauthors = Botzenhart E, Vester U, Schmidt C, Hesse A, Halber M, Wagner C, Lang F, Hoyer P, Zerres K, Eggermann T | title = Cystinuria in children: distribution and frequencies of mutations in the SLC3A1 and SLC7A9 genes | journal = Kidney Int. | volume = 62 | issue = 4 | pages = 1136–1142 | year = 2003 | pmid = 12234283 | doi = 10.1111/j.1523-1755.2002.kid552.x | doi-access = free }}
 {{refend}}
-{{membrane-protein-stub}}
 {{Solute carrier family|bg|bg0}}
 [[Category:Solute carrier family]]
+{{membrane-protein-stub}}

Latest revision as of 12:56, 4 January 2024

See also[edit]

References[edit]

Further reading[edit]