Homo sapiens dihydropyrimidine dehydrogenase (DPYD), transcript varian - Nucleotide

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MIR27A rs895819 TC genotype increases risk of fluoropyrimidine-induced severe toxicity independently of DPYD variations. [Pharmacogenomics. 2024]
MIR27A rs895819 TC genotype increases risk of fluoropyrimidine-induced severe toxicity independently of DPYD variations.
Ragia G, Biziota E, Koukaki T, Amarantidis K, Manolopoulos VG. Pharmacogenomics. 2024 Jan; 25(2):59-67. Epub 2024 Feb 14.
Integrating rare genetic variants into DPYD pharmacogenetic testing may help preventing fluoropyrimidine-induced toxicity. [Pharmacogenomics J. 2024]
Integrating rare genetic variants into DPYD pharmacogenetic testing may help preventing fluoropyrimidine-induced toxicity.
Larrue R, Fellah S, Hennart B, Sabaouni N, Boukrout N, Van der Hauwaert C, Delage C, Cheok M, Perrais M, Cauffiez C, et al. Pharmacogenomics J. 2024 Jan 12; 24(1):1. Epub 2024 Jan 12.
Common dihydropyrimidinase ( DPYS ) genetic variations do not predict fluoropyrimidine-related chemotherapy toxicity in a Canadian cohort. [Pharmacogenet Genomics. 2024]
Common dihydropyrimidinase ( DPYS ) genetic variations do not predict fluoropyrimidine-related chemotherapy toxicity in a Canadian cohort.
Medwid SJ, Mailloux JL, Wigle TJ, Kim RB. Pharmacogenet Genomics. 2024 Apr 1; 34(3):83-87. Epub 2024 Jan 15.

RefSeq alternative splicing
See 11 reference mRNA sequence splice variants for the DPYD gene.
RefSeq protein product
See the reference protein sequence for dihydropyrimidine dehydrogenase (NP_001153773.1).

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Protein sequence from Nucleotide coding region
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Nucleotide