Gene: UGT1A1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 54658
Gene Symbol: UGT1A1
UGT1A1 		0.070 GeneticVariation phenotype BEFREE The role of UGT1A1 promoter polymorphism and exon-1 mutations in neonatal jaundice. 27842454 2017
Entrez Id: 54658
Gene Symbol: UGT1A1
UGT1A1 		0.070 GeneticVariation phenotype BEFREE Gene Mutation in Neonatal Jaundice - Mutations in UGT1A1 and OATP2 Genes. 26960716 2016
Entrez Id: 54658
Gene Symbol: UGT1A1
UGT1A1 		0.070 GeneticVariation phenotype BEFREE Mutation of the UGT1A1 gene, glycine to arginine at codon 71 (G71R), is related to the development of neonatal jaundice in East Asian populations but the frequency of this mutation is rare among Caucasian populations. 20528217 2011
Entrez Id: 54658
Gene Symbol: UGT1A1
UGT1A1 		0.070 GeneticVariation phenotype BEFREE Polymorphic variants of UGT1A1 in neonatal jaundice in southern Brazil. 20061399 2010
Entrez Id: 54658
Gene Symbol: UGT1A1
UGT1A1 		0.070 GeneticVariation phenotype BEFREE In conclusion, the c.-3279T>G mutation in the UGT1A1 promoter is a genetic risk factor for neonatal jaundice. 20057336 2010
Entrez Id: 54658
Gene Symbol: UGT1A1
UGT1A1 		0.070 Biomarker phenotype BEFREE In this study we examined the effects of OSM on CAR-mediated signaling to investigate its potential role in neonatal jaundice via the CAR-UGT1A1 pathway. 20197307 2010
Entrez Id: 54658
Gene Symbol: UGT1A1
UGT1A1 		0.070 GeneticVariation phenotype BEFREE (TA)7 allele frequency was 0.069 and it is concluded that UGT1A1 promoter region polymorphism was not a risk factor for neonatal jaundice. 17166930 2007