rs397978903
|
UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
|
Crigler Najjar syndrome, type 2
|
|
0.700 |
GeneticVariation |
UNIPROT |
Identification of a novel mutation in UDP-glucuronosyltransferase (UGT1A1) gene in a child with neonatal unconjugated hyperbilirubinemia.
|
23099197 |
2013 |
rs397978903
|
UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
|
Crigler Najjar syndrome, type 2
|
|
0.700 |
GeneticVariation |
UNIPROT |
UGT1A1 gene mutations in Pakistani children suffering from inherited nonhemolytic unconjugated hyperbilirubinemias.
|
23992562 |
2013 |
rs397978903
|
UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
|
Crigler Najjar syndrome, type 2
|
|
0.700 |
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 |
rs397978903
|
UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
|
Crigler Najjar syndrome, type 2
|
|
0.700 |
GeneticVariation |
UNIPROT |
Influence of mutations associated with Gilbert and Crigler-Najjar type II syndromes on the glucuronidation kinetics of bilirubin and other UDP-glucuronosyltransferase 1A substrates.
|
18004206 |
2007 |
rs397978903
|
UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
|
Crigler Najjar syndrome, type 2
|
|
0.700 |
GeneticVariation |
UNIPROT |
Seven novel mutations of the UGT1A1 gene in patients with unconjugated hyperbilirubinemia.
|
17229650 |
2007 |
rs397978903
|
UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
|
Crigler Najjar syndrome, type 2
|
|
0.700 |
GeneticVariation |
UNIPROT |
Spectrum of UGT1A1 mutations in Crigler-Najjar (CN) syndrome patients: identification of twelve novel alleles and genotype-phenotype correlation.
|
15712364 |
2005 |
rs397978903
|
UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
|
Crigler Najjar syndrome, type 2
|
|
0.700 |
GeneticVariation |
UNIPROT |
Rapid proteasomal degradation of translocation-deficient UDP-glucuronosyltransferase 1A1 proteins in patients with Crigler-Najjar type II.
|
14550264 |
2003 |
rs397978903
|
UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
|
Crigler Najjar syndrome, type 2
|
|
0.700 |
GeneticVariation |
UNIPROT |
Association of a homozygous (TA)8 promoter polymorphism and a N400D mutation of UGT1A1 in a child with Crigler-Najjar type II syndrome.
|
12402338 |
2002 |
rs397978903
|
UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
|
Crigler Najjar syndrome, type 2
|
|
0.700 |
GeneticVariation |
UNIPROT |
Interaction of coding region mutations and the Gilbert-type promoter abnormality of the UGT1A1 gene causes moderate degrees of unconjugated hyperbilirubinaemia and may lead to neonatal kernicterus.
|
11370628 |
2001 |
rs397978903
|
UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
|
Crigler Najjar syndrome, type 2
|
|
0.700 |
GeneticVariation |
UNIPROT |
Genetic lesions of bilirubin uridine-diphosphoglucuronate glucuronosyltransferase (UGT1A1) causing Crigler-Najjar and Gilbert syndromes: correlation of genotype to phenotype.
|
11013440 |
2000 |
rs397978903
|
UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
|
Crigler Najjar syndrome, type 2
|
|
0.700 |
GeneticVariation |
UNIPROT |
Analysis of bilirubin uridine 5'-diphosphate (UDP)-glucuronosyltransferase gene mutations in seven patients with Crigler-Najjar syndrome type II.
|
9621515 |
1998 |
rs397978903
|
UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
|
Crigler Najjar syndrome, type 2
|
|
0.700 |
GeneticVariation |
UNIPROT |
Coding defect and a TATA box mutation at the bilirubin UDP-glucuronosyltransferase gene cause Crigler-Najjar type I disease.
|
9639672 |
1998 |
rs397978903
|
UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
|
Crigler Najjar syndrome, type 2
|
|
0.700 |
GeneticVariation |
UNIPROT |
A mutation which disrupts the hydrophobic core of the signal peptide of bilirubin UDP-glucuronosyltransferase, an endoplasmic reticulum membrane protein, causes Crigler-Najjar type II.
|
8706880 |
1996 |
rs397978903
|
UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
|
Crigler Najjar syndrome, type 2
|
|
0.700 |
GeneticVariation |
UNIPROT |
Discrimination between Crigler-Najjar type I and II by expression of mutant bilirubin uridine diphosphate-glucuronosyltransferase.
|
7989595 |
1994 |
rs397978903
|
UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
|
Crigler Najjar syndrome, type 2
|
|
0.700 |
GeneticVariation |
UNIPROT |
Identification of an A-to-G missense mutation in exon 2 of the UGT1 gene complex that causes Crigler-Najjar syndrome type 2.
|
8276413 |
1993 |
rs397978903
|
UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
|
Crigler Najjar syndrome, type 2
|
|
0.700 |
GeneticVariation |
UNIPROT |
Identification of defect in the genes for bilirubin UDP-glucuronosyl-transferase in a patient with Crigler-Najjar syndrome type II.
|
8280139 |
1993 |