Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 8542
Gene Symbol: APOL1
APOL1
0.080 Biomarker disease BEFREE This case supports the role of IFN in inducing APOL1-associated collapsing glomerulopathy. 31601430 2020
Entrez Id: 8542
Gene Symbol: APOL1
APOL1
0.080 GeneticVariation disease BEFREE Donor's APOL1 Risk Genotype and "Second Hits" Associated With De Novo Collapsing Glomerulopathy in Deceased Donor Kidney Transplant Recipients: A Report of 5 Cases. 30054024 2019
Entrez Id: 8542
Gene Symbol: APOL1
APOL1
0.080 Biomarker disease BEFREE Expanding the spectrum of APOL1-related renal disease: de novo collapsing glomerulopathy following kidney transplant. 30466562 2018
Entrez Id: 8542
Gene Symbol: APOL1
APOL1
0.080 GeneticVariation disease BEFREE Donor APOL1 high-risk genotypes are associated with increased risk and inferior prognosis of de novo collapsing glomerulopathy in renal allografts. 30287079 2018
Entrez Id: 8542
Gene Symbol: APOL1
APOL1
0.080 GeneticVariation disease BEFREE These findings support the causative role of parvovirus B19 infection in the development of CG on the background of APOL1 genetic risk. 27600725 2016
Entrez Id: 8542
Gene Symbol: APOL1
APOL1
0.080 Biomarker disease BEFREE Immunity unmasks APOL1 in collapsing glomerulopathy. 25635718 2015
Entrez Id: 8542
Gene Symbol: APOL1
APOL1
0.080 GeneticVariation disease BEFREE In conclusion, APOL1 genotyping of African-American patients with SLE might help identify patients at risk for collapsing glomerulopathy, an entity with a poor prognosis that is often resistant to treatment. 23520206 2013
Entrez Id: 8542
Gene Symbol: APOL1
APOL1
0.080 GeneticVariation disease BEFREE We describe here for the first time the association of CG in a young Afro-American female with SLE having a homozygous mutation of APOL1. 22952321 2012
Entrez Id: 84942
Gene Symbol: WDR73
WDR73
0.010 GeneticVariation disease BEFREE This study extended the clinical and molecular spectrum of GAMOS1 with other cases associated with collapsing glomerulopathy and two novel WDR73 variations that are most likely pathogenic. 30315938 2019
Entrez Id: 10891
Gene Symbol: PPARGC1A
PPARGC1A
0.010 AlteredExpression disease BEFREE Increasing PGC-1α levels in podocytes induces podocyte proliferation and collapsing glomerulopathy development, while increasing PGC1-α in endothelial cells alters endothelial function and causes microangiopathy, thus highlighting the cell-type-specific role of PGC-1α in different kidney cells. 29602395 2018
Entrez Id: 5468
Gene Symbol: PPARG
PPARG
0.010 AlteredExpression disease BEFREE Increasing the level of peroxisome proliferator-activated receptor γ coactivator-1α in podocytes results in collapsing glomerulopathy. 28724797 2017
Entrez Id: 57107
Gene Symbol: PDSS2
PDSS2
0.010 GeneticVariation disease BEFREE The mouse gene Pdss2 is mutated in the kd/kd mouse model of collapsing glomerulopathy. 23926186 2013
Entrez Id: 7015
Gene Symbol: TERT
TERT
0.010 AlteredExpression disease BEFREE Transgenic TERT expression in mice induces marked upregulation of Wnt signaling and disrupts glomerular structure, resulting in a collapsing glomerulopathy resembling those in human disease, including HIV-associated nephropathy (HIVAN). 22138751 2011
Entrez Id: 6876
Gene Symbol: TAGLN
TAGLN
0.010 AlteredExpression disease BEFREE Along with SM22α induction in PHN, confirmed at both mRNA and protein levels, SM22α was also induced across a broad range of proteinuric diseases, including experimental animal models (puromycin aminonucleoside nephropathy, adriamycin nephropathy, passive nephrotoxic nephritis, and diet-induced obesity) and human diseases (collapsing glomerulopathy, diabetic nephropathy, classic focal segmental glomerulosclerosis, IgA nephropathy, minimal-change disease, membranous nephropathy, and membranoproliferative glomerulonephritis). 21289056 2011
Entrez Id: 7133
Gene Symbol: TNFRSF1B
TNFRSF1B
0.010 AlteredExpression disease BEFREE We detected de novo expression of TNFR2 on podocytes before hyperplastic injury in crescentic glomerulonephritis of mice with nephrotoxic nephritis, and in collapsing glomerulopathy of Tg26(HIV/nl) mice, kd/kd mice, and human beings. 21221075 2011
Entrez Id: 4627
Gene Symbol: MYH9
MYH9
0.010 GeneticVariation disease BEFREE Admixture mapping identified genetic variants in the nonmuscle myosin heavy chain 9 gene (MYH9) as having a major influence on both FSGS and human immunodeficiency virus-associated collapsing glomerulopathy, with odds ratios from 4 to 8 and attributable fractions of 70% to 100%. 20347641 2010
Entrez Id: 81
Gene Symbol: ACTN4
ACTN4
0.010 GeneticVariation disease BEFREE Most adult homozygous Actn4 mutant and knockout mice developed collapsing glomerulopathy. 18185509 2008