APOL1, apolipoprotein L1, 8542

N. diseases: 115; N. variants: 9
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases
0.100 Biomarker group BEFREE No evidence for association between APOL1 kidney disease risk alleles and Human African Trypanosomiasis in two Ugandan populations. 29470556 2018
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases
0.100 Biomarker group BEFREE These include: (1) the intra-renal renin-angiotensin system (RAS), one based on molecular variations in angiotensinogen; (2) the Na, K, 2Cl cotransporter (NKCC2) and its regulators in the thick ascending limb, which are associated with a variety of phenotypes consistent with a more active cotransporter in blacks; and (3) the genes for MYH9 and APOL 1, which have been associated with kidney disease in blacks. 23397215 2013
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases
0.100 GeneticVariation group BEFREE Some of the most striking findings relate to APOL1 genetic variants, seen exclusively in individuals of sub-Saharan African descent, that create a predisposition to particular renal disorders, including focal segmental glomerulosclerosis and arterionephrosclerosis. 30082052 2018
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases
0.100 GeneticVariation group BEFREE Urinary JCPyV was associated with paradoxically lower rates of nephropathy in those with APOL1 high-risk genotypes. 30320619 2019
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases
0.100 Biomarker group BEFREE Here, we discuss the possibility that abnormal efflux of cellular potassium or other cations may be relevant to the pathogenesis of APOL1 nephropathy. 29110762 2017
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases
0.100 GeneticVariation group BEFREE We sought to evaluate the cardiovascular impact of coding variants in the apolipoprotein L1 gene APOL1 that protect against trypanosome infection but have been associated with kidney disease among African Americans. 26634651 2016
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases
0.100 GeneticVariation group BEFREE Genome-wide association studies have identified a substantial signal at 22q13, now assigned to variation at apolipoprotein L1 (APOL1), which has associated with progressive nondiabetic nephropathy, cardiovascular disease, and many immune-associated renal diseases, including lupus nephritis. 28265848 2017
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases
0.100 GeneticVariation group BEFREE For example, the G1 and G2 variants of the APOL1 gene supporting control of Trypanosoma infection come with the trade-off that they promote the progression of kidney disease. 28481398 2017
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases
0.100 Biomarker group BEFREE MYH9 and APOL1 are both associated with sickle cell disease nephropathy. 21910715 2011
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases
0.100 GeneticVariation group BEFREE Homozygosity for apolipoprotein-L1 (APOL1) risk variants has emerged as an important predictor of renal disease in individuals of African descent over the past several years. 27588375 2016
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases
0.100 Biomarker group BEFREE Gene-gene interactions in APOL1-associated nephropathy. 24157943 2014
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases
0.100 Biomarker group BEFREE This article reviews the current status of APOL1-associated nephropathy and discusses research questions under active investigation in the search for a cure for these severe and often progressive kidney diseases. 24119848 2013
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases
0.100 Biomarker group BEFREE Since HIVAN has the strongest association with APOL1 genotype of any of the APOL1-associated nephropathies, studies to determine the mechanisms by which HIV and APOL1 risk variants together promote kidney injury hold great promise to improve our understanding of the pathogenesis of APOL1-mediated kidney diseases. 29930940 2018
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases
0.100 GeneticVariation group BEFREE APOL1 risk variants have been shown to be strongly associated with an increased risk for non-diabetic kidney disease including HIV nephropathy, primary non-monogenic focal and segmental glomerulosclerosis, and hypertension-attributed nephropathy among African ancestry populations in the USA. 23860441 2013
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases
0.100 GeneticVariation group BEFREE We conclude that variation in APOL1 G3 makes a nominal, if any, contribution to ESRD in African Americans; G1 and G2 variants explain the vast majority of nondiabetic nephropathy susceptibility. 25249559 2015
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases
0.100 GeneticVariation group BEFREE In this study, we examined the effects of overexpressing wild-type (G0) and kidney disease risk variants (G1 and G2) of APOL1 in human podocytes using a lentivirus expression system. 24899058 2014
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases
0.100 GeneticVariation group BEFREE APOL1 G1/G2 variants are the strongest genetic predictors of kidney disease in the general African-American population. 26206798 2015
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases
0.100 Biomarker group BEFREE Transcript analysis of mouse kidney disease models, including folic-acid (FA)-induced nephropathy, unilateral ureteral obstruction (UUO), or apolipoprotein L1 (APOL1)-associated kidney disease, indicated that Jag1 and Notch2 levels were higher in all analyzed kidney fibrosis models. 30226866 2018
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases
0.100 GeneticVariation group BEFREE Kidneys from African American deceased donors with two APOL1 nephropathy variants reproducibly associate with higher risk for allograft failure after transplantation. 25809272 2015
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases
0.100 Biomarker group BEFREE Our study not only reveals the contribution of each domain of the APOL1 protein to cell injury, but also highlights some potential suggested targets for drug design to prevent or treat APOL1-associated nephropathy. 26091559 2015
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases
0.100 Biomarker group BEFREE Detection of APOL1 associations with kidney diseases and delineation of injury pathways brings hope for effective treatment for these kidney diseases. 30343724 2018
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases
0.100 GeneticVariation group BEFREE APOL1 genotypes are associated with kidney diseases in African American individuals and may influence cardiovascular disease and mortality risk, but findings have been inconsistent. 29971324 2018
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases
0.100 GeneticVariation group BEFREE In populations of African ancestry, two <i>apolipoprotein-L1 (APOL1</i>) variants with a recessive kidney disease risk, named G1 and G2, occur at high frequency. 28537557 2017
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases
0.100 Biomarker group BEFREE Heterogeneity in study population and study design has led to differing reports on the role of APOL1 nephropathy risk variants in CVD. 31082862 2019
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases
0.100 Biomarker group BEFREE The linkage peak on chromosome 22q overlaps the MYH9/APOL1 gene region, previously implicated in AA diabetic and nondiabetic nephropathies. 21454968 2011