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. Author manuscript; available in PMC: 2012 Apr 1.
Published in final edited form as: Pharmacogenet Genomics. 2011 Apr;21(4):237–242. doi: 10.1097/FPC.0b013e32833c6107

Fig. 1.

Fig. 1

Graphic representation of the candidate genes involved in fluoropyrimidine pharmacokinetics. A fully interactive version of this pathway is available online at PharmGKB at http://www.pharmgkb.org/do/serve?objId=PA150653776&objCls=Pathway. 5′-dFCR, 5′-deoxy-5-fluorocytidine; 5′-dFUR, 5′-deoxy-5-fluorouridine; 5-FU, 5-fluorouracil; ABCC, ATP-binding cassette, sub-family C; CDA, cytidine deaminase; CES, carboxylesterase; DHFU, dihydrofluorouracil; DPYD, dihydropyrimidine dehydrogenase’; DPYS, dihydropyrimidinease; FBAL, fluoro-β-alanine; FdUDP, fluorodeoxyuridine diphosphate; FdUMP, fluorodeoxyuridine monophosphate; FdUTP, fluoro-deoxyuridine triphosphate; FUDP, fluorouridine diphosphate; FUDR, fluorodeoxyuridine; FUMP, fluorouridine monophosphate; FUPA, fluoro-β-ureidopropionate; FUR, fluroridine; FUTP, fluorouridine triphosphate; PD, pharmacodynamic; PPAT, phosphoribosyl pyrophosphate amidotransferase; RRM, ribonucleotide reductase M; TK1, thymidine kinase 1; Tp53, tumor protein p53; TYMP, thymidylate phosphorylase; TYMS, thymidylate synthase; UCK, uridine-cytidine kinase; UMPS, uridine monophosphate synthase; UPB1, β-ureidopropionase 1; UPP, uridine phosphorylase.