UCSF Pharmacogenetics of Membrane Transporters
Snp Publications
PMT SNP UID:4069
  1. Liu R, Tang AM, Tan YL, Limenta LM, Lee EJ. Interethnic differences of PEPT2 (SLC15A2) polymorphism distribution and associations with cephalexin pharmacokinetics in healthy Asian subjects. Eur J Clin Pharmacol. 2009 Jan;65(1):65-70. PMID: 18766334.
  2. Sala-Rabanal M, Loo DD, Hirayama BA, Wright EM. Molecular mechanism of dipeptide and drug transport by the human renal H+/oligopeptide cotransporter hPEPT2. Am J Physiol Renal Physiol. 2008 Jun;294(6):F1422-32. PMID: 18367661.
  3. Pinsonneault J, Nielsen CU, Sadée W. Genetic variants of the human H+/dipeptide transporter PEPT2: analysis of haplotype functions. J Pharmacol Exp Ther. 2004 Dec;311(3):1088-96. PMID: 15282265.
  4. Terada T, Irie M, Okuda M, Inui K. Genetic variant Arg57His in human H+/peptide cotransporter 2 causes a complete loss of transport function. Biochem Biophys Res Commun. 2004 Apr 2;316(2):416-20. PMID: 15020234.