Skip Header

You are using a version of browser that may not display all the features of this website. Please consider upgrading your browser.
1 to 25 of 576  Show
  1. 1
    "A novel missence mutation A664S in exon 1 of human UGT1A1 gene."
    Rathi R., Prasad R., Khullar N., Kumar P.
    Submitted (FEB-2012) to the EMBL/GenBank/DDBJ databases
    Cited for: NUCLEOTIDE SEQUENCE.
    Category: Sequences.
    Source: UniProtKB/TrEMBL (unreviewed).
  2. 2
    "Association of neonatal hyperbilirubinemia with bilirubin UDP-glucuronosyltransferase polymorphism."
    Maruo Y., Nishizawa K., Sato H., Doida Y., Shimada M.
    Pediatrics 103:1224-1227(1999) [PubMed] [Europe PMC] [Abstract]
    Category: Pathology & Biotech.
    Annotation: Associated with METABOLIC: neonatal hyperbilirubinemia.
    Source: GAD:142087.

    This publication is mapped to 23 other entries.

  3. 3
    "Distribution of the A(TA)7TAA genotype associated with Gilbert syndrome in the Spanish population."
    Fernandez Salazar J.M., Remacha Sevilla A., del Rio Conde E., Baiget Bastus M.
    Med Clin (Barc) 115:540-541(2000) [PubMed] [Europe PMC] [Abstract]
    Category: Sequences.
    Annotation: Observational study of genotype prevalence. (HuGE Navigator).
    Source: GeneRIF:54658.

    This publication is mapped to 24 other entries.

  4. 4
    "Polymorphisms of UDP-glucuronosyltransferase gene and irinotecan toxicity: a pharmacogenetic analysis."
    Ando Y., Saka H., Ando M., Sawa T., Muro K., Ueoka H., Yokoyama A., Saitoh S., Shimokata K., Hasegawa Y.
    Cancer Res. 60:6921-6926(2000) [PubMed] [Europe PMC] [Abstract]
    Category: Function, Pathology & Biotech.
    Annotation: Associated with PHARMACOGENOMIC: irinotecan toxicity. [GAD:142089]. Observational study of gene-environment interaction. (HuGE Navigator). [GeneRIF:54658].
    Source: GeneRIF:54658, GAD:142089.

    This publication is mapped to 24 other entries.

  5. 5
    "Association of genetic polymorphisms in UGT1A1 with breast cancer and plasma hormone levels."
    Guillemette C., De Vivo I., Hankinson S.E., Haiman C.A., Spiegelman D., Housman D.E., Hunter D.J.
    Cancer Epidemiol. Biomarkers Prev. 10:711-714(2001) [PubMed] [Europe PMC] [Abstract]
    Category: Function, Pathology & Biotech.
    Annotation: Not Associated with CANCER: breast cancer; hormone levels. [GAD:142090]. Observational study of gene-disease association. (HuGE Navigator). [GeneRIF:54658].
    Source: GAD:142090, GeneRIF:54658.

    This publication is mapped to 24 other entries.

  6. 6
    Category: Pathology & Biotech, Sequences.
    Annotation: Observational study of gene-disease association. (HuGE Navigator). [GeneRIF:54658]. Associated with METABOLIC: Gilbert's syndrome. [GAD:142118].
    Source: GAD:142118, GeneRIF:54658.

    This publication is mapped to 24 other entries.

  7. 7
    "[Interest in the study of genetic variants of the promoter region of the UGT1A1 gene in neonatal jaundice]."
    Seco M.L., del Rio E., Barcelo M.J., Remacha A., Ginovart G., Moliner E., Baiget M.
    An. Esp. Pediatr. 56:139-143(2002) [PubMed] [Europe PMC] [Abstract]
    Category: Sequences.
    Annotation: Observational study of gene-disease association. (HuGE Navigator).
    Source: GeneRIF:54658.

    This publication is mapped to 24 other entries.

  8. 8
    "A novel intronic mutation results in the use of a cryptic splice acceptor site within the coding region of UGT1A1, causing Crigler-Najjar syndrome type 1."
    Sappal B.S., Ghosh S.S., Shneider B., Kadakol A., Chowdhury J.R., Chowdhury N.R.
    Mol. Genet. Metab. 75:134-142(2002) [PubMed] [Europe PMC] [Abstract]
    Category: Sequences.
    Annotation: A novel G > A mutation at the splice acceptor site in intron 4 causing Crigler-Najjar syndrome type 1.
    Source: GeneRIF:54658.

    This publication is mapped to 24 other entries.

  9. 9
    "Frequencies of UDP-glucuronosyltransferase 1 (UGT1A1) gene promoter polymorphisms among distinct ethnic groups from Brazil."
    Fertrin K.Y., Goncalves M.S., Saad S.T., Costa F.F.
    Am. J. Med. Genet. 108:117-119(2002) [PubMed] [Europe PMC] [Abstract]
    Category: Sequences.
    Annotation: Observational study of genotype prevalence. (HuGE Navigator); The high frequencies of (TA)(7) polymorphism among the three groups confirm previous data that this polymorphism is very ancient and appears to be distributed throughout the world.
    Source: GeneRIF:54658.

    This publication is mapped to 24 other entries.

  10. 10
    "Influence of bilirubin uridine diphosphate-glucuronosyltransferase 1A promoter polymorphisms on serum bilirubin levels and cholelithiasis in children with sickle cell anemia."
    Passon R.G., Howard T.A., Zimmerman S.A., Schultz W.H., Ware R.E.
    J. Pediatr. Hematol. Oncol. 23:448-451(2001) [PubMed] [Europe PMC] [Abstract]
    Category: Function, Pathology & Biotech, Sequences.
    Annotation: Polymorphisms in UGT1A1 causes cholelithiasis and a modifier of bilirubin metabolism; Observational study of gene-disease association. (HuGE Navigator). [GeneRIF:54658]. Associated with METABOLIC: cholelithiasis; bilirubin. [GAD:142092].
    Source: GAD:142092, GeneRIF:54658.

    This publication is mapped to 24 other entries.

  11. 11
    "Identification of a defect in the UGT1A1 gene promoter and its association with hyperbilirubinemia."
    Sugatani J., Yamakawa K., Yoshinari K., Machida T., Takagi H., Mori M., Kakizaki S., Sueyoshi T., Negishi M., Miwa M.
    Biochem. Biophys. Res. Commun. 292:492-497(2002) [PubMed] [Europe PMC] [Abstract]
    Category: Function, Pathology & Biotech, Sequences.
    Annotation: polymorphism in the UGT1A1 gene promoter and its association with hyperbilirubinemia; Observational study of gene-disease association. (HuGE Navigator). [GeneRIF:54658]. Associated with METABOLIC: hyperbilirubinemia. [GAD:142120, GAD:142088].
    Source: GAD:142120, GeneRIF:54658, GAD:142088.

    This publication is mapped to 24 other entries.

  12. 12
    "Hemolysis and bilirubin conjugation in association with UDP-glucuronosyltransferase 1A1 promoter polymorphism."
    Kaplan M., Hammerman C., Rubaltelli F.F., Vilei M.T., Levy-Lahad E., Renbaum P., Vreman H.J., Stevenson D.K., Muraca M.
    Hepatology 35:905-911(2002) [PubMed] [Europe PMC] [Abstract]
    Category: Function, Pathology & Biotech, Sequences.
    Annotation: Observational study of gene-disease association. (HuGE Navigator). [GeneRIF:54658]. Associated with METABOLIC: bilirubin; hemolysis. [GAD:142093].
    Source: GeneRIF:54658, GAD:142093.

    This publication is mapped to 24 other entries.

  13. 13
    "Genotyping by"cold single-strand conformation polymorphism" of the UGT1A1 promoter polymorphism in Mexican mestizos."
    Arambula E., Vaca G.
    Blood Cells Mol. Dis. 28:86-90(2002) [PubMed] [Europe PMC] [Abstract]
    Category: Sequences.
    Annotation: Observational study of genotype prevalence and genetic testing. (HuGE Navigator).
    Source: GeneRIF:54658.

    This publication is mapped to 24 other entries.

  14. 14
    "Genetic polymorphisms of the UDP-glucuronosyltransferase 1A7 gene and irinotecan toxicity in Japanese cancer patients."
    Ando M., Ando Y., Sekido Y., Ando M., Shimokata K., Hasegawa Y.
    Jpn. J. Cancer Res. 93:591-597(2002) [PubMed] [Europe PMC] [Abstract]
    Category: Function, Pathology & Biotech, Expression, Sequences.
    Annotation: Observational study of gene-disease association gene-environment interaction and pharmacogenomic / toxicogenomic. (HuGE Navigator). [GeneRIF:54658]. Not Associated with PHARMACOGENOMIC: irinotecan toxicity. [GAD:142095].
    Source: GeneRIF:54658, GAD:142095.

    This publication is mapped to 24 other entries.

  15. 15
    "Predicting the risk of sporadic elevated bilirubin levels and diagnosing Gilbert's syndrome by genotyping UGT1A1*28 promoter polymorphism."
    Rauchschwalbe S.K., Zuhlsdorf M.T., Schuhly U., Kuhlmann J.
    Int J Clin Pharmacol Ther 40:233-240(2002) [PubMed] [Europe PMC] [Abstract]
    Category: Sequences.
    Annotation: Observational study of gene-disease association. (HuGE Navigator).
    Source: GeneRIF:54658.

    This publication is mapped to 24 other entries.

  16. 16
    "Glucose-6-phosphate dehydrogenase deficiency, the UDP-glucuronosyl transferase 1A1 gene, and neonatal hyperbilirubinemia."
    Huang C.S., Chang P.F., Huang M.J., Chen E.S., Chen W.C.
    Gastroenterology 123:127-133(2002) [PubMed] [Europe PMC] [Abstract]
    Category: Pathology & Biotech, Sequences.
    Annotation: Associated with METABOLIC: hyperbilirubinemia. [GAD:142121]. Observational study of gene-disease association. (HuGE Navigator); results indicate that carriage of the homozygous 211 G to A variation within the coding region is an additive risk factor for neonatal hyperbilirubinemia in G6PD-deficient Taiwanese male neonates. [GeneRIF:54658].
    Source: GAD:142121, GeneRIF:54658.

    This publication is mapped to 24 other entries.

  17. 17
    "Sulforaphane and its glutathione conjugate but not sulforaphane nitrile induce UDP-glucuronosyl transferase (UGT1A1) and glutathione transferase (GSTA1) in cultured cells."
    Basten G.P., Bao Y., Williamson G.
    Carcinogenesis 23:1399-1404(2002) [PubMed] [Europe PMC] [Abstract]
    Category: Function.
    Annotation: induction in cultured tumor cells by sulforaphane and its glutathione conjugate.
    Source: GeneRIF:54658.

    This publication is mapped to 24 other entries.

  18. 18
    "Morphine glucuronide-to-morphine plasma ratios are unaffected by the UGT2B7 H268Y and UGT1A1*28 polymorphisms in cancer patients on chronic morphine therapy."
    Holthe M., Klepstad P., Zahlsen K., Borchgrevink P.C., Hagen L., Dale O., Kaasa S., Krokan H.E., Skorpen F.
    Eur. J. Clin. Pharmacol. 58:353-356(2002) [PubMed] [Europe PMC] [Abstract]
    Category: Function, Pathology & Biotech.
    Annotation: Observational study of gene-environment interaction and pharmacogenomic / toxicogenomic. (HuGE Navigator). [GeneRIF:54658]. Not Associated with CANCER: cancer. [GAD:142116].
    Source: GAD:142116, GeneRIF:54658.

    This publication is mapped to 30 other entries.

  19. 19
    "Relationship between bilirubin UDP-glucuronosyl transferase 1A1 gene and neonatal hyperbilirubinemia."
    Huang C.S., Chang P.F., Huang M.J., Chen E.S., Hung K.L., Tsou K.I.
    Pediatr. Res. 52:601-605(2002) [PubMed] [Europe PMC] [Abstract]
    Category: Pathology & Biotech, Sequences.
    Annotation: Associated with METABOLIC: hyperbilirubinemia. [GAD:142122]. Observational study of gene-disease association. (HuGE Navigator). [GeneRIF:54658].
    Source: GeneRIF:54658, GAD:142122.

    This publication is mapped to 24 other entries.

  20. 20
    "Coinheritance of variant UDP-glucuronosyl transferase 1A1 gene and glucose-6-phosphate dehydrogenase deficiency in adults with hyperbilirubinemia."
    Huang M.J., Yang Y.C., Yang S.S., Lin M.S., Chen E.S., Huang C.S.
    Pharmacogenetics 12:663-666(2002) [PubMed] [Europe PMC] [Abstract]
    Category: Sequences.
    Annotation: Observational study of gene-gene interaction. (HuGE Navigator).
    Source: GeneRIF:54658.

    This publication is mapped to 44 other entries.

  21. 21
    "Combined polymorphisms in UDP-glucuronosyltransferases 1A1 and 1A6: implications for patients with Gilbert's syndrome."
    Peters W.H., te Morsche R.H., Roelofs H.M.
    J. Hepatol. 38:3-8(2003) [PubMed] [Europe PMC] [Abstract]
    Category: Function, Pathology & Biotech.
    Annotation: Most patients with Gilbert's syndrome may have abnormalities in glucuronidation of aspirin or coumarin- and dopamine-derivatives due to this combination of UGT1A1*28 and UGT1A6*2 genotypes; Observational study of gene-disease association. (HuGE Navigator). [GeneRIF:54658]. Associated with METABOLIC: Gilbert syndrome. [GAD:142113].
    Source: GAD:142113, GeneRIF:54658.

    This publication is mapped to 31 other entries.

  22. 22
    "Inherited disorders of bilirubin metabolism."
    Bosma P.J.
    J. Hepatol. 38:107-117(2003) [PubMed] [Europe PMC] [Abstract]
    Category: Function.
    Annotation: Crigler Najar syndrome and Gilbert syndrome caused by deficiency in hepatic glucuronidation of bilirubin resulting from mutation of UGTqA1 gene. (review).
    Source: GeneRIF:54658.

    This publication is mapped to 24 other entries.

  23. 23
    "[A study of polymorphism in UDP-glucuronosyltransferase 1 (UGT-1A1) promoter gene in Korean patients with Gilbert's syndrome]."
    Kim Y.H., Yeon J.E., Jung G.M., Kim H.J., Kim J.S., Byun K.S., Bak Y.T., Lee C.H.
    Taehan Kan Hakhoe Chi 8:132-138(2002) [PubMed] [Europe PMC] [Abstract]
    Category: Pathology & Biotech, Sequences.
    Annotation: Not Associated with METABOLIC: Gilbert syndrome. [GAD:142097]. Observational study of gene-disease association. (HuGE Navigator). [GeneRIF:54658].
    Source: GeneRIF:54658, GAD:142097.

    This publication is mapped to 24 other entries.

  24. 24
    "Gly71Arg mutation of the bilirubin UDP-glucuronosyltransferase 1A1 gene is associated with neonatal hyperbilirubinemia in the Japanese population."
    Yamamoto A., Nishio H., Waku S., Yokoyama N., Yonetani M., Uetani Y., Nakamura H.
    Kobe J Med Sci 48:73-77(2002) [PubMed] [Europe PMC] [Abstract]
    Category: Pathology & Biotech, Sequences.
    Annotation: Associated with METABOLIC: hyperbilirubinemia. [GAD:142123]. Observational study of gene-disease association. (HuGE Navigator). [GeneRIF:54658].
    Source: GeneRIF:54658, GAD:142123.

    This publication is mapped to 24 other entries.

  25. 25
    "Involvement of the xenobiotic response element (XRE) in Ah receptor-mediated induction of human UDP-glucuronosyltransferase 1A1."
    Yueh M.F., Huang Y.H., Hiller A., Chen S., Nguyen N., Tukey R.H.
    J. Biol. Chem. 278:15001-15006(2003) [PubMed] [Europe PMC] [Abstract]
    Category: Sequences.
    Annotation: UGT1A1 induction by ligand binding to the Ah receptor was regionalized to a UGT1A1 enhancer region containing a xenobiotic response element (XRE) at -3381/-3299.
    Source: GeneRIF:54658.

    This publication is mapped to 27 other entries.

1 to 25 of 576  Show
UniProt is an ELIXIR core data resource
Main funding by: National Institutes of Health

We'd like to inform you that we have updated our Privacy Notice to comply with Europe’s new General Data Protection Regulation (GDPR) that applies since 25 May 2018.

Do not show this banner again