Type | Description |
---|---|
Definition | dihydropyrimidine dehydrogenase |
Date | Results | Publications |
---|---|---|
2021-03-27 14:45:00 | Evaluation of adverse effects of chemotherapy regimens of 5-fluoropyrimidines derivatives and their association with DPYD polymorphisms in colorectal cancer patients. | 32546132 |
2021-02-20 13:33:00 | New DPYD variants causing DPD deficiency in patients treated with fluoropyrimidine. | 32529295 |
2020-07-11 11:52:00 | In updated analysis of cohort of patients with gastrointestinal malignancies treated with fluoropyrimidines, the prevalence of heterozygous and homozygous DPYD*9A genotypes were 41% and 10%, respectively. The correlation between DPYD*9A genotype and dihydropyrimidine dehydrogenase deficiency clinical phenotype was not reproduced. Previously reported correlation is likely because of small sample size and selection bias. | 31160238 |
2020-05-16 13:07:00 | A significant association was observed between DPYD*9A polymorphism and apecitabine and Oxaliplatin (CAPOX) associated toxicities in colorectal cancer patients. | 31653159 |
2019-11-16 13:32:00 | Prospective DPYD genotyping can be successfully implemented in routine clinical practice and can reduce the risk of severe fluoropyrimidine toxicities | 30746637 |
Type | IDs |
---|---|
Synonymous | DHP, DHPDHASE, DPD |
Gene |
UniProtKB-ID:
DPYD_HUMAN
UniprotKB:
Q12882
UniParc:
UPI000006D155,
UPI00000727C7
EMBL:
AC138135,
CH471097,
AC114878,
AC099787,
BC131777,
AB003063,
AL356457,
BC008379,
AK291217,
BT006740,
U57655,
U09178,
BC108742,
U20938,
AC093576,
BX908805,
AC091608,
BC064027,
X95670,
BC131778
Ensembl:
ENSG00000188641
KO:
hsa:1806
|
Nucleutide sequences |
EMBL-CDS:
CAA64973.1,
BAA89789.1,
AAB07049.1,
AAI08743.1,
EAW73002.1,
BAF83906.1,
AAI31779.1,
AAH64027.1,
AAH08379.1,
AAB51366.1,
AAP35386.1,
AAA57474.1,
AAI31778.1
Ensembl_TRS:
ENST00000370192,
ENST00000306031
|
Protein sequencees |
Ensembl_PRO:
ENSP00000359211,
ENSP00000307107
RefSeq:
XP_016855997.1,
XP_016855996.1,
NP_001153773.1,
XP_005270619.2,
XP_016855998.1,
XP_016855999.1,
XP_006710460.1,
NP_000101.2
|
Others |
UniRef100:
UniRef100_Q12882
UniRef90:
UniRef90_Q12882
UniRef50:
UniRef50_Q12882
UniGene:
Hs.335034
CCDS:
CCDS53346.1,
CCDS30777.1
|
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Refseq |
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