SLC14A1

SLC14A1

Solute carrier family 14 (urea transporter), member 1 (Kidd blood group), also known as SLC14A1, is a human gene.cite web | title = Entrez Gene: SLC14A1 solute carrier family 14 (urea transporter), member 1 (Kidd blood group)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=6563| accessdate = ]

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ee also

* Solute carrier family

References

Further reading

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citations =
*cite journal | author=Geitvik GA, Høyheim B, Gedde-Dahl T, "et al." |title=The Kidd (JK) blood group locus assigned to chromosome 18 by close linkage to a DNA-RFLP. |journal=Hum. Genet. |volume=77 |issue= 3 |pages= 205–9 |year= 1987 |pmid= 2890568 |doi=
*cite journal | author=Olivès B, Mattei MG, Huet M, "et al." |title=Kidd blood group and urea transport function of human erythrocytes are carried by the same protein. |journal=J. Biol. Chem. |volume=270 |issue= 26 |pages= 15607–10 |year= 1995 |pmid= 7797558 |doi=
*cite journal | author=Olives B, Neau P, Bailly P, "et al." |title=Cloning and functional expression of a urea transporter from human bone marrow cells. |journal=J. Biol. Chem. |volume=269 |issue= 50 |pages= 31649–52 |year= 1995 |pmid= 7989337 |doi=
*cite journal | author=Davey S, Beach D |title=RACH2, a novel human gene that complements a fission yeast cell cycle checkpoint mutation. |journal=Mol. Biol. Cell |volume=6 |issue= 10 |pages= 1411–21 |year= 1996 |pmid= 8573795 |doi=
*cite journal | author=Olivès B, Martial S, Mattei MG, "et al." |title=Molecular characterization of a new urea transporter in the human kidney. |journal=FEBS Lett. |volume=386 |issue= 2-3 |pages= 156–60 |year= 1996 |pmid= 8647271 |doi=
*cite journal | author=Olivès B, Merriman M, Bailly P, "et al." |title=The molecular basis of the Kidd blood group polymorphism and its lack of association with type 1 diabetes susceptibility. |journal=Hum. Mol. Genet. |volume=6 |issue= 7 |pages= 1017–20 |year= 1997 |pmid= 9215669 |doi=
*cite journal | author=Lucien N, Sidoux-Walter F, Olivès B, "et al." |title=Characterization of the gene encoding the human Kidd blood group/urea transporter protein. Evidence for splice site mutations in Jknull individuals. |journal=J. Biol. Chem. |volume=273 |issue= 21 |pages= 12973–80 |year= 1998 |pmid= 9582331 |doi=
*cite journal | author=Irshaid NM, Thuresson B, Olsson ML |title=Genomic typing of the Kidd blood group locus by a single-tube allele-specific primer PCR technique. |journal=Br. J. Haematol. |volume=102 |issue= 4 |pages= 1010–4 |year= 1998 |pmid= 9734652 |doi=
*cite journal | author=Sidoux-Walter F, Lucien N, Olivès B, "et al." |title=At physiological expression levels the Kidd blood group/urea transporter protein is not a water channel. |journal=J. Biol. Chem. |volume=274 |issue= 42 |pages= 30228–35 |year= 1999 |pmid= 10514515 |doi=
*cite journal | author=Irshaid NM, Henry SM, Olsson ML |title=Genomic characterization of the kidd blood group gene:different molecular basis of the Jk(a-b-) phenotype in Polynesians and Finns. |journal=Transfusion |volume=40 |issue= 1 |pages= 69–74 |year= 2000 |pmid= 10644814 |doi=
*cite journal | author=Sidoux-Walter F, Lucien N, Nissinen R, "et al." |title=Molecular heterogeneity of the Jk(null) phenotype: expression analysis of the Jk(S291P) mutation found in Finns. |journal=Blood |volume=96 |issue= 4 |pages= 1566–73 |year= 2000 |pmid= 10942407 |doi=
*cite journal | author=Lucien N, Chiaroni J, Cartron JP, Bailly P |title=Partial deletion in the JK locus causing a Jk(null) phenotype. |journal=Blood |volume=99 |issue= 3 |pages= 1079–81 |year= 2002 |pmid= 11807016 |doi=
*cite journal | author=Irshaid NM, Eicher NI, Hustinx H, "et al." |title=Novel alleles at the JK blood group locus explain the absence of the erythrocyte urea transporter in European families. |journal=Br. J. Haematol. |volume=116 |issue= 2 |pages= 445–53 |year= 2002 |pmid= 11841450 |doi=
*cite journal | author=Lucien N, Sidoux-Walter F, Roudier N, "et al." |title=Antigenic and functional properties of the human red blood cell urea transporter hUT-B1. |journal=J. Biol. Chem. |volume=277 |issue= 37 |pages= 34101–8 |year= 2002 |pmid= 12093813 |doi= 10.1074/jbc.M205073200
*cite journal | author=Strausberg RL, Feingold EA, Grouse LH, "et al." |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899
*cite journal | author=Ota T, Suzuki Y, Nishikawa T, "et al." |title=Complete sequencing and characterization of 21,243 full-length human cDNAs. |journal=Nat. Genet. |volume=36 |issue= 1 |pages= 40–5 |year= 2004 |pmid= 14702039 |doi= 10.1038/ng1285
*cite journal | author=Inoue H, Jackson SD, Vikulina T, "et al." |title=Identification and characterization of a Kidd antigen/UT-B urea transporter expressed in human colon. |journal=Am. J. Physiol., Cell Physiol. |volume=287 |issue= 1 |pages= C30–5 |year= 2004 |pmid= 14985236 |doi= 10.1152/ajpcell.00443.2003

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