DPYD
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DPYD is one of the key pharmacogenes involved in the implementation of pharmacogenomics.
- It is involved in guidelines for fluorouracil and capecitabine (go to list of all guidelines with DPYD).
- the nomenclature has been set by PharmVar
- the key variants are tier 1 DPYD c.1905+1G>A (*2A), DPYD c.1679T>G (*13), DPYD c.1129-5923C>G, c.1236G>A (HapB3), DPYD c.557A>G, DPYD c.868A>G, DPYD c.2279C>T, DPYD c.2846A>T , and tier 2 DPYD c.295_298delTCAT (*7), DPYD c.703C>T (*8), DPYD c.1314T>G, DPYD c.1475C>T, DPYD c.1774C>T,DPYD c.2639G>T [Article:39032821] see all alleles on the AMP recommended to test list.
- See the Gene-specific Information Tables for Allele Definitions (for which variants comprise which star alleles), Allele function assignments (normal function, no function, decreased or increased function etc) and Diplotype-Phenotype Table (for how the alleles combine to form metabolizer phenotypes for PM, NM, UM)
Location
Strand | Minus |
Cytogenetic | chr1 : p21.3 - p21.3 |
GRCh37 | chr1 : 97543299 - 98386615 |
GRCh38 | chr1 : 97077743 - 97921059 |
Names & Symbols
ID
HGNC Approved Name
Alternate Names
- Dihydrothymine dehydrogenase
- Dihydrouracil dehydrogenase
Alternate Symbols
- DHPDHase
- DPD