Protein-coding gene in the species Homo sapiens
SLC14A1 Identifiers Aliases SLC14A1 , HUT11, HsT1341, JK, RACH1, RACH2, UT-B1, UT1, UTE, solute carrier family 14 member 1 (Kidd blood group), Jk(b), HUT11A, Jk(a)External IDs OMIM : 613868 ; MGI : 1351654 ; HomoloGene : 9285 ; GeneCards : SLC14A1 ; OMA :SLC14A1 - orthologs Wikidata
Urea transporter 1 is a protein that in humans is encoded by the SLC14A1 gene .[ 5] [ 6]
The SLC14A1 codes for a urea transporter (UTB) that is expressed in erythrocytes and kidney . SLC14A2 and SLC14A1 constitute solute carrier family 14. UTB proteins constitute the Kidd antigen system .
^ a b c GRCh38: Ensembl release 89: ENSG00000141469 – Ensembl , May 2017
^ a b c GRCm38: Ensembl release 89: ENSMUSG00000059336 – 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 .
^ Olives B, Mattei MG, Huet M, Neau P, Martial S, Cartron JP, Bailly P (Aug 1995). "Kidd blood group and urea transport function of human erythrocytes are carried by the same protein" . J Biol Chem . 270 (26): 15607–10. doi :10.1074/jbc.270.26.15607 . PMID 7797558 .
^ "Entrez Gene: SLC14A1 solute carrier family 14 (urea transporter), member 1 (Kidd blood group)" .
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. doi :10.1007/BF00284470 . PMID 2890568 . S2CID 23739401 .
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. doi :10.1016/S0021-9258(18)31744-7 . PMID 7989337 .
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. doi :10.1091/mbc.6.10.1411 . PMC 301296 . PMID 8573795 .
Olivès B, Martial S, Mattei MG, et al. (1996). "Molecular characterization of a new urea transporter in the human kidney" (PDF) . FEBS Lett . 386 (2–3): 156–60. doi :10.1016/0014-5793(96)00425-5 . PMID 8647271 . S2CID 13312002 .
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. doi :10.1093/hmg/6.7.1017 . PMID 9215669 .
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. doi :10.1074/jbc.273.21.12973 . PMID 9582331 .
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. doi :10.1046/j.1365-2141.1998.00874.x . PMID 9734652 . S2CID 19082798 .
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. doi :10.1074/jbc.274.42.30228 . hdl :2066/185970 . PMID 10514515 .
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. doi :10.1046/j.1537-2995.2000.40010069.x . PMID 10644814 . S2CID 43843439 .
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. doi :10.1182/blood.V96.4.1566 . PMID 10942407 .
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. doi :10.1182/blood.V99.3.1079 . PMID 11807016 .
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. doi :10.1046/j.1365-2141.2002.03238.x . PMID 11841450 . S2CID 25830269 .
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 .
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. Bibcode :2002PNAS...9916899M . doi :10.1073/pnas.242603899 . PMC 139241 . PMID 12477932 .
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 .
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 . S2CID 25576221 .
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human Na+ -sulfate/carboxylate cotransporter
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monocarboxylate transporter
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SLC21–30
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Na+-dependent ascorbic acid transporter
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Na+ -coupled nucleoside transport (SLC28A1
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facilitative nucleoside transporter
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SLC31–40
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type II Na+ -phosphate cotransporter
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nucleoside-sugar transporter
SLC35E1
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sugar-phosphate/phosphate exchanger
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System A & N, sodium-coupled neutral amino-acid transporter
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basolateral iron transporter
SLC41–48
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Na+ -independent, system-L like amino-acid transporter
(44): (45):
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(46): (47): (48):