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Solute carrier family 15 (H+/peptide transporter), member 2
Identifiers
Symbols SLC15A2; PEPT2
External IDs OMIM602339 MGI1890457 HomoloGene56912 GeneCards: SLC15A2 Gene
RNA expression pattern
PBB GE SLC15A2 205317 s at tn.png
PBB GE SLC15A2 205316 at tn.png
More reference expression data
Orthologs
Species Human Mouse
Entrez 6565 57738
Ensembl ENSG00000163406 ENSMUSG00000022899
UniProt Q16348 Q80XC0
RefSeq (mRNA) NM_021082 NM_021301
RefSeq (protein) NP_066568 NP_067276
Location (UCSC) Chr 3:
123.1 - 123.14 Mb
Chr 16:
36.67 - 36.7 Mb
PubMed search [1] [2]

Solute carrier family 15 (H+/peptide transporter), member 2, also known as SLC15A2, is a human gene.[1]

See also

References

Further reading

  • Liu W, Liang R, Ramamoorthy S, et al. (1995). "Molecular cloning of PEPT 2, a new member of the H+/peptide cotransporter family, from human kidney.". Biochim. Biophys. Acta 1235 (2): 461–6. doi:10.1016/0005-2736(95)80036-F. PMID 7756356.  
  • Döring F, Martini C, Walter J, Daniel H (2002). "Importance of a small N-terminal region in mammalian peptide transporters for substrate affinity and function.". J. Membr. Biol. 186 (2): 55–62. doi:10.1007/s00232-001-0135-9. PMID 11944083.  
  • Alcorn J, Lu X, Moscow JA, McNamara PJ (2002). "Transporter gene expression in lactating and nonlactating human mammary epithelial cells using real-time reverse transcription-polymerase chain reaction.". J. Pharmacol. Exp. Ther. 303 (2): 487–96. doi:10.1124/jpet.102.038315. PMID 12388627.  
  • 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.  
  • Groneberg DA (2003). "[Expression, localization and functional aspects of the peptide transporter PEPT2 in the normal respiratory tract and in cystic fibrosis]". Pneumologie (Stuttgart, Germany) 57 (2): 104–5. doi:10.1055/s-2003-37158. PMID 12579467.  
  • Terada T, Irie M, Okuda M, Inui K (2004). "Genetic variant Arg57His in human H+/peptide cotransporter 2 causes a complete loss of transport function.". Biochem. Biophys. Res. Commun. 316 (2): 416–20. doi:10.1016/j.bbrc.2004.02.063. PMID 15020234.  
  • Pinsonneault J, Nielsen CU, Sadée W (2005). "Genetic variants of the human H+/dipeptide transporter PEPT2: analysis of haplotype functions.". J. Pharmacol. Exp. Ther. 311 (3): 1088–96. doi:10.1124/jpet.104.073098. PMID 15282265.  
  • Bahadduri PM, D'Souza VM, Pinsonneault JK, et al. (2005). "Functional characterization of the peptide transporter PEPT2 in primary cultures of human upper airway epithelium.". Am. J. Respir. Cell Mol. Biol. 32 (4): 319–25. doi:10.1165/rcmb.2004-0322OC. PMID 15626774.  
  • Zhang EY, Emerick RM, Pak YA, et al. (2005). "Comparison of human and monkey peptide transporters: PEPT1 and PEPT2.". Mol. Pharm. 1 (3): 201–10. doi:10.1021/mp0499712. PMID 15981923.  
  • Noshiro R, Anzai N, Sakata T, et al. (2006). "The PDZ domain protein PDZK1 interacts with human peptide transporter PEPT2 and enhances its transport activity.". Kidney Int. 70 (2): 275–82. doi:10.1038/sj.ki.5001522. PMID 16738539.  
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