Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3162
Gene Symbol: HMOX1
HMOX1
0.270 GeneticVariation disease BEFREE The results of this study indicate that there is a significant association between the HMOX1 (GT)<sub>n</sub> repeat length polymorphism and susceptibility to neonatal hyperbilirubinemia. 30700176 2019
Entrez Id: 3162
Gene Symbol: HMOX1
HMOX1
0.270 GeneticVariation disease BEFREE Additionally, multivariate logistic regression analysis identified that the mutant genotype of rs4148323 in the UGT1A1 gene, ABO incompatibility, G6PD deficiency, and SS genotype at rs1805173 locus of the HO-1 gene were genetic risk factors of neonatal hyperbilirubinemia. 30298137 2018
Entrez Id: 3162
Gene Symbol: HMOX1
HMOX1
0.270 GeneticVariation disease BEFREE In this clinical review, we surveyed the role of HO-1 gene promoter polymorphisms in the control of bilirubin production and further considered their role, if any, in the pathophysiology of neonatal hyperbilirubinemia. 28206992 2017
Entrez Id: 3162
Gene Symbol: HMOX1
HMOX1
0.270 GeneticVariation disease BEFREE G6PD deficiency, short HO-1 promoter GT-repeat and GA at nt211 in UGT1A1 are risk factors of neonatal hyperbilirubinemia. 27557546 2016
Entrez Id: 3162
Gene Symbol: HMOX1
HMOX1
0.270 GeneticVariation disease BEFREE Short (GT)n repeats of HO-1 gene, c.211G>A variant of UGT1A1 gene, and excessive weight loss were independent risk factors for neonatal hyperbilirubinemia. 23877636 2013
Entrez Id: 3162
Gene Symbol: HMOX1
HMOX1
0.270 Biomarker disease RGD Targeted suppression of heme oxygenase-1 by small interference RNAs inhibits the production of bilirubin in neonatal rat with hyperbilirubinemia. 19646271 2009
Entrez Id: 3162
Gene Symbol: HMOX1
HMOX1
0.270 GeneticVariation disease BEFREE Because bilirubin production plays a critical role during the neonatal period, the HO-1 promoter polymorphism may be an important genetic factor for the clinical outcome of neonatal hyperbilirubinemia. 17325212 2007
Entrez Id: 3162
Gene Symbol: HMOX1
HMOX1
0.270 GeneticVariation disease BEFREE Neonatal hyperbilirubinemia in Japanese neonates: analysis of the heme oxygenase-1 gene and fetal hemoglobin composition in cord blood. 12736395 2003