Type | Description |
---|---|
Definition | UDP glucuronosyltransferase family 1 member A4 |
Date | Results | Publications |
---|---|---|
2021-02-20 13:28:00 | The association of genetic polymorphisms in CYP1A2, UGT1A4, and ABCB1 with autonomic nervous system dysfunction in schizophrenia patients treated with olanzapine. | 32070304 |
2020-11-21 13:33:00 | Representation of CYP3A4, CYP3A5 and UGT1A4 Polymorphisms within Croatian Breast Cancer Patients' Population. | 32456253 |
2020-09-19 16:27:00 | Association of CYP2C19 and UGT1A4 polymorphisms with voriconazole-induced liver injury. | 31797717 |
2020-04-18 10:12:00 | Chinese patients with A/A or G/A genotype in the promoter region of bilirubin glucuronoside glucuronosyltransferase (UGT1A4) have a lower 5-year disease-free survival (DFS) rate than those with the wild-type G/G genotype when treated with adjuvant tamoxifen. The rs869283 genotype remains an independent prognostic marker for DFS in multivariate analysis. | 30630678 |
2019-01-19 11:45:00 | Genetic polymorphism in UGT1A4 and UGT2B7 may play a modest role in lamotrigine clearance changes during pregnancy. In addition, study indicates that the sex of the foetus influenced significantly the change in LTG clearance. | 29395496 |
Type | IDs |
---|---|
Synonymous | GNT1, HUG-BR2, UDPGT, UDPGT 1-4, UGT-1A, UGT-1D, UGT1, UGT1-01, UGT1-04, UGT1.1, UGT1.4, UGT1A, UGT1A1, UGT1A4S, UGT1D, hUG-BR1 |
Gene |
UniProtKB-ID:
UD14_HUMAN
UniprotKB:
P22310
UniParc:
UPI0000001044,
UPI000173A5DC
EMBL:
M84128,
M84122,
CH471063,
AC006985,
AY435139,
AF297093,
AK313623,
M84124,
M57951,
AC114812,
BC139784,
DQ364249,
M84123
Ensembl:
ENSG00000244474
KO:
hsa:54657
|
Nucleutide sequences |
EMBL-CDS:
AAA61247.1,
ABC96773.1,
AAA63196.1,
AAI39785.1,
BAG36384.1,
EAW71061.1,
AAR95640.1,
AAG30422.1,
AAA61249.1
Ensembl_TRS:
ENST00000373409,
ENST00000450233
|
Protein sequencees |
Ensembl_PRO:
ENSP00000362508,
ENSP00000408608
RefSeq:
NP_009051.1
|
Others |
UniRef100:
UniRef100_P22310
UniRef90:
UniRef90_P22310
UniRef50:
UniRef50_P35503
UniGene:
Hs.554822
CCDS:
CCDS33405.1
|
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Refseq |
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