Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 10661
Gene Symbol: KLF1
KLF1
0.080 GeneticVariation group BEFREE With the aim of determining the role of KLF1 gene variations in HbF induction and their genotype phenotype relationship, in this study, we screened 370 individuals with different hemoglobinopathy condition. 30529538 2019
Entrez Id: 10661
Gene Symbol: KLF1
KLF1
0.080 GeneticVariation group BEFREE This study aimed to investigate whether KLF1 mutation can associate with high level of HbF in individuals with increased fetal hemoglobin referred for screening of hemoglobinopathies in south of Iran. 29420372 2018
Entrez Id: 10661
Gene Symbol: KLF1
KLF1
0.080 GeneticVariation group BEFREE Here we report a novel KLF1 gene variation codon 211 A→G (c.632 A>G) in a family who was referred for hemoglobinopathy screening. 28369821 2017
Entrez Id: 10661
Gene Symbol: KLF1
KLF1
0.080 GeneticVariation group BEFREE Mutations in the gene encoding EKLF may cause hemoglobinopathies, such as hereditary persistence of fetal hemoglobin and β-thalassemia intermedia, and congenital dyserythropoietic anemia type IV, which is a hematopoietic disorder. 27708211 2016
Entrez Id: 10661
Gene Symbol: KLF1
KLF1
0.080 AlteredExpression group BEFREE KLF1 is therefore an important genetic factor associated with increased Hb F and in combination with other modifying factors could explain the phenotypic variation of Hb F expression in this common hemoglobinopathy. 27282573 2016
Entrez Id: 10661
Gene Symbol: KLF1
KLF1
0.080 GeneticVariation group BEFREE KLF1 mutations are important in a screening program for hemoglobinopathies. 26794457 2016
Entrez Id: 10661
Gene Symbol: KLF1
KLF1
0.080 GeneticVariation group BEFREE This supports the emerging concept that monoallelic KLF1 mutations can play a modulatory role in hemoglobinopathies. 25082863 2014
Entrez Id: 10661
Gene Symbol: KLF1
KLF1
0.080 Biomarker group BEFREE These results suggest that strategies designed to antagonize EKLF function in adults with hemoglobinopathy, in an attempt to reactivate gamma-globin gene expression, may adversely affect other essential aspects of red blood cell physiology.(Blood.2000;95:1827-1833) 10688844 2000