Disease: Crigler Najjar syndrome, type 1 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs62625011
rs62625011
Entrez Id: 54575;54576;54577;54578;54579;54600;54657;54658;54659
Gene Symbol: UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
CUI: C0010324
Disease:
Crigler Najjar syndrome, type 1 		0.810 GeneticVariation UNIPROT UGT1A1 gene mutations in Pakistani children suffering from inherited nonhemolytic unconjugated hyperbilirubinemias. 23992562 2013
dbSNP: rs62625011
rs62625011
Entrez Id: 54575;54576;54577;54578;54579;54600;54657;54658;54659
Gene Symbol: UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
CUI: C0010324
Disease:
Crigler Najjar syndrome, type 1 		0.810 GeneticVariation UNIPROT Crigler-Najjar syndrome in The Netherlands: identification of four novel UGT1A1 alleles, genotype-phenotype correlation, and functional analysis of 10 missense mutants. 19830808 2010
dbSNP: rs62625011
rs62625011
Entrez Id: 54575;54576;54577;54578;54579;54600;54657;54658;54659
Gene Symbol: UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
CUI: C0010324
Disease:
Crigler Najjar syndrome, type 1 		0.810 GeneticVariation UNIPROT Seven novel mutations of the UGT1A1 gene in patients with unconjugated hyperbilirubinemia. 17229650 2007
dbSNP: rs62625011
rs62625011
Entrez Id: 54575;54576;54577;54578;54579;54600;54657;54658;54659
Gene Symbol: UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
CUI: C0010324
Disease:
Crigler Najjar syndrome, type 1 		0.810 GeneticVariation BEFREE Prenatal diagnosis in a family with a boy previously diagnosed as Crigler-Najjar syndrome type I and homozygosity for the c.923G>A mutation revealed that the fetus was unaffected. 16269258 2006
dbSNP: rs62625011
rs62625011
Entrez Id: 54575;54576;54577;54578;54579;54600;54657;54658;54659
Gene Symbol: UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
CUI: C0010324
Disease:
Crigler Najjar syndrome, type 1 		0.810 GeneticVariation UNIPROT Spectrum of UGT1A1 mutations in Crigler-Najjar (CN) syndrome patients: identification of twelve novel alleles and genotype-phenotype correlation. 15712364 2005
dbSNP: rs62625011
rs62625011
Entrez Id: 54575;54576;54577;54578;54579;54600;54657;54658;54659
Gene Symbol: UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
CUI: C0010324
Disease:
Crigler Najjar syndrome, type 1 		0.810 GeneticVariation UNIPROT Genetic lesions of bilirubin uridine-diphosphoglucuronate glucuronosyltransferase (UGT1A1) causing Crigler-Najjar and Gilbert syndromes: correlation of genotype to phenotype. 11013440 2000
dbSNP: rs62625011
rs62625011
Entrez Id: 54575;54576;54577;54578;54579;54600;54657;54658;54659
Gene Symbol: UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
CUI: C0010324
Disease:
Crigler Najjar syndrome, type 1 		0.810 GeneticVariation UNIPROT Identification of two single base substitutions in the UGT1 gene locus which abolish bilirubin uridine diphosphate glucuronosyltransferase activity in vitro. 7906695 1994
dbSNP: rs62625011
rs62625011
Entrez Id: 54575;54576;54577;54578;54579;54600;54657;54658;54659
Gene Symbol: UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
CUI: C0010324
Disease:
Crigler Najjar syndrome, type 1 		0.810 GeneticVariation UNIPROT Here, we report eleven mutations (including nine novel mutations) of the B-UGT1 gene in a large series of 14 unrelated CN-I children of various geographic origins: France (seven patients: A401P, Q357X, W335X, A368T, 1223insG, A291V, K426E, K437X); Portugal (two patients: G308E); Tunisia (two patients; Q357R); Turkey (one patient: S381R); italy (two siblings: S381R). 7989045 1994
dbSNP: rs62625011
rs62625011
Entrez Id: 54575;54576;54577;54578;54579;54600;54657;54658;54659
Gene Symbol: UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
CUI: C0010324
Disease:
Crigler Najjar syndrome, type 1 		0.810 GeneticVariation UNIPROT Discrimination between Crigler-Najjar type I and II by expression of mutant bilirubin uridine diphosphate-glucuronosyltransferase. 7989595 1994
dbSNP: rs62625011
rs62625011
Entrez Id: 54575;54576;54577;54578;54579;54600;54657;54658;54659
Gene Symbol: UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
CUI: C0010324
Disease:
Crigler Najjar syndrome, type 1 		0.810 GeneticVariation UNIPROT A phenylalanine codon deletion at the UGT1 gene complex locus of a Crigler-Najjar type I patient generates a pH-sensitive bilirubin UDP-glucuronosyltransferase. 8226884 1993
dbSNP: rs62625011
rs62625011
Entrez Id: 54575;54576;54577;54578;54579;54600;54657;54658;54659
Gene Symbol: UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
CUI: C0010324
Disease:
Crigler Najjar syndrome, type 1 		0.810 GeneticVariation UNIPROT Mechanisms of inherited deficiencies of multiple UDP-glucuronosyltransferase isoforms in two patients with Crigler-Najjar syndrome, type I. 1634050 1992
dbSNP: rs62625011
rs62625011
Entrez Id: 54575;54576;54577;54578;54579;54600;54657;54658;54659
Gene Symbol: UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
CUI: C0010324
Disease:
Crigler Najjar syndrome, type 1 		A 0.810 CausalMutation CLINVAR