SLC14A1

Solute carrier family 14 (urea transporter), member 1 (Kidd blood group)
Identifiers
Symbols	SLC14A1 ; FLJ33745; FLJ41687; HUT11; HsT1341; JK; RACH1; UT-B1; UT1; UTE
External IDs	Template:OMIM5 Template:MGI HomoloGene: 9285
Gene ontology Molecular function Template:GNF GO Template:GNF GO Cellular component Template:GNF GO Template:GNF GO Template:GNF GO Biological process Template:GNF GO Template:GNF GO Template:GNF GO
RNA expression pattern
File:PBB GE SLC14A1 205856 at tn.png
More reference expression data
Orthologs
Template:GNF Ortholog box
Species	Human	Mouse
Entrez	n/a	n/a
Ensembl	n/a	n/a
UniProt	n/a	n/a
RefSeq (mRNA)	n/a	n/a
RefSeq (protein)	n/a	n/a
Location (UCSC)	n/a	n/a
PubMed search	n/a	n/a

Solute carrier family 14 (urea transporter), member 1 (Kidd blood group), also known as SLC14A1, is a human gene.

See also

• Solute carrier family

Further reading

• Geitvik GA, Høyheim B, Gedde-Dahl T; et al. (1987). "The Kidd (JK) blood group locus assigned to chromosome 18 by close linkage to a DNA-RFLP". Hum. Genet. 77 (3): 205–9. PMID 2890568.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Olivès B, Mattei MG, Huet M; et al. (1995). "Kidd blood group and urea transport function of human erythrocytes are carried by the same protein". J. Biol. Chem. 270 (26): 15607–10. PMID 7797558.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Olives B, Neau P, Bailly P; et al. (1995). "Cloning and functional expression of a urea transporter from human bone marrow cells". J. Biol. Chem. 269 (50): 31649–52. PMID 7989337.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Davey S, Beach D (1996). "RACH2, a novel human gene that complements a fission yeast cell cycle checkpoint mutation". Mol. Biol. Cell. 6 (10): 1411–21. PMID 8573795.
• Olivès B, Martial S, Mattei MG; et al. (1996). "Molecular characterization of a new urea transporter in the human kidney". FEBS Lett. 386 (2–3): 156–60. PMID 8647271.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Olivès B, Merriman M, Bailly P; et al. (1997). "The molecular basis of the Kidd blood group polymorphism and its lack of association with type 1 diabetes susceptibility". Hum. Mol. Genet. 6 (7): 1017–20. PMID 9215669.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Lucien N, Sidoux-Walter F, Olivès B; et al. (1998). "Characterization of the gene encoding the human Kidd blood group/urea transporter protein. Evidence for splice site mutations in Jknull individuals". J. Biol. Chem. 273 (21): 12973–80. PMID 9582331.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Irshaid NM, Thuresson B, Olsson ML (1998). "Genomic typing of the Kidd blood group locus by a single-tube allele-specific primer PCR technique". Br. J. Haematol. 102 (4): 1010–4. PMID 9734652.CS1 maint: Multiple names: authors list (link)
• Sidoux-Walter F, Lucien N, Olivès B; et al. (1999). "At physiological expression levels the Kidd blood group/urea transporter protein is not a water channel". J. Biol. Chem. 274 (42): 30228–35. PMID 10514515.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Irshaid NM, Henry SM, Olsson ML (2000). "Genomic characterization of the kidd blood group gene:different molecular basis of the Jk(a-b-) phenotype in Polynesians and Finns". Transfusion. 40 (1): 69–74. PMID 10644814.CS1 maint: Multiple names: authors list (link)
• Sidoux-Walter F, Lucien N, Nissinen R; et al. (2000). "Molecular heterogeneity of the Jk(null) phenotype: expression analysis of the Jk(S291P) mutation found in Finns". Blood. 96 (4): 1566–73. PMID 10942407.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Lucien N, Chiaroni J, Cartron JP, Bailly P (2002). "Partial deletion in the JK locus causing a Jk(null) phenotype". Blood. 99 (3): 1079–81. PMID 11807016.CS1 maint: Multiple names: authors list (link)
• Irshaid NM, Eicher NI, Hustinx H; et al. (2002). "Novel alleles at the JK blood group locus explain the absence of the erythrocyte urea transporter in European families". Br. J. Haematol. 116 (2): 445–53. PMID 11841450.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Lucien N, Sidoux-Walter F, Roudier N; et al. (2002). "Antigenic and functional properties of the human red blood cell urea transporter hUT-B1". J. Biol. Chem. 277 (37): 34101–8. doi:10.1074/jbc.M205073200. PMID 12093813.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Strausberg RL, Feingold EA, Grouse LH; et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMID 12477932.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Ota T, Suzuki Y, Nishikawa T; et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID 14702039.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Inoue H, Jackson SD, Vikulina T; et al. (2004). "Identification and characterization of a Kidd antigen/UT-B urea transporter expressed in human colon". Am. J. Physiol., Cell Physiol. 287 (1): C30–5. doi:10.1152/ajpcell.00443.2003. PMID 14985236.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)