Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7490
Gene Symbol: WT1
WT1 		0.400 GeneticVariation disease CLINVAR
Entrez Id: 51479
Gene Symbol: ANKFY1
ANKFY1 		0.300 GermlineCausalMutation disease ORPHANET GAPVD1 and ANKFY1 Mutations Implicate RAB5 Regulation in Nephrotic Syndrome. 29959197 2018
Entrez Id: 26130
Gene Symbol: GAPVD1
GAPVD1 		0.300 GermlineCausalMutation disease ORPHANET GAPVD1 and ANKFY1 Mutations Implicate RAB5 Regulation in Nephrotic Syndrome. 29959197 2018
Entrez Id: 7827
Gene Symbol: NPHS2
NPHS2 		0.610 CausalMutation disease CLINVAR A molecular genetic analysis of childhood nephrotic syndrome in a cohort of Saudi Arabian families. 23595123 2013
Entrez Id: 126859
Gene Symbol: AXDND1
AXDND1 		0.100 CausalMutation disease CLINVAR A molecular genetic analysis of childhood nephrotic syndrome in a cohort of Saudi Arabian families. 23595123 2013
Entrez Id: 7225
Gene Symbol: TRPC6
TRPC6 		0.300 GermlineCausalMutation disease ORPHANET A mutation in the TRPC6 cation channel causes familial focal segmental glomerulosclerosis. 15879175 2005
Entrez Id: 7827
Gene Symbol: NPHS2
NPHS2 		0.610 CausalMutation disease CLINVAR A novel mutation in NPHS2 gene identified in a Chinese pedigree with autosomal recessive steroid-resistant nephrotic syndrome. 20001346 2009
Entrez Id: 7827
Gene Symbol: NPHS2
NPHS2 		0.610 GeneticVariation disease CLINVAR A novel mutation of NPHS2 identified in a Chinese family. 15322893 2004
Entrez Id: 7827
Gene Symbol: NPHS2
NPHS2 		0.610 CausalMutation disease CLINVAR A novel mutation of NPHS2 identified in a Chinese family. 15322893 2004
Entrez Id: 7490
Gene Symbol: WT1
WT1 		0.400 GermlineCausalMutation disease ORPHANET A novel WT1 gene mutation in a three-generation family with progressive isolated focal segmental glomerulosclerosis. 20150449 2010
Entrez Id: 8542
Gene Symbol: APOL1
APOL1 		0.300 SusceptibilityMutation disease ORPHANET A risk allele for focal segmental glomerulosclerosis in African Americans is located within a region containing APOL1 and MYH9. 20668430 2010
Entrez Id: 8542
Gene Symbol: APOL1
APOL1 		0.300 SusceptibilityMutation disease ORPHANET A role for genetic susceptibility in sporadic focal segmental glomerulosclerosis. 26901816 2016
Entrez Id: 7827
Gene Symbol: NPHS2
NPHS2 		0.610 CausalMutation disease CLINVAR A single-gene cause in 29.5% of cases of steroid-resistant nephrotic syndrome. 25349199 2015
Entrez Id: 7827
Gene Symbol: NPHS2
NPHS2 		0.610 GeneticVariation disease CLINVAR A single-gene cause in 29.5% of cases of steroid-resistant nephrotic syndrome. 25349199 2015
Entrez Id: 126859
Gene Symbol: AXDND1
AXDND1 		0.100 CausalMutation disease CLINVAR A single-gene cause in 29.5% of cases of steroid-resistant nephrotic syndrome. 25349199 2015
Entrez Id: 126859
Gene Symbol: AXDND1
AXDND1 		0.100 GeneticVariation disease CLINVAR A single-gene cause in 29.5% of cases of steroid-resistant nephrotic syndrome. 25349199 2015
Entrez Id: 7827
Gene Symbol: NPHS2
NPHS2 		0.610 CausalMutation disease CLINVAR A spectrum of novel NPHS1 and NPHS2 gene mutations in pediatric nephrotic syndrome patients from Pakistan. 22565185 2012
Entrez Id: 126859
Gene Symbol: AXDND1
AXDND1 		0.100 CausalMutation disease CLINVAR A spectrum of novel NPHS1 and NPHS2 gene mutations in pediatric nephrotic syndrome patients from Pakistan. 22565185 2012
Entrez Id: 79934
Gene Symbol: COQ8B
COQ8B 		0.300 GermlineCausalMutation disease ORPHANET ADCK4 mutations promote steroid-resistant nephrotic syndrome through CoQ10 biosynthesis disruption. 24270420 2013
Entrez Id: 7827
Gene Symbol: NPHS2
NPHS2 		0.610 GeneticVariation disease CLINVAR Analysis of NPHS1, NPHS2, ACTN4, and WT1 in Japanese patients with congenital nephrotic syndrome. 15780077 2005
Entrez Id: 7827
Gene Symbol: NPHS2
NPHS2 		0.610 GeneticVariation disease CLINVAR Analysis of NPHS2 mutations in Turkish steroid-resistant nephrotic syndrome patients. 16810518 2006
Entrez Id: 7827
Gene Symbol: NPHS2
NPHS2 		0.610 GeneticVariation disease CLINVAR Anemia in congenital nephrotic syndrome: role of urinary copper and ceruloplasmin loss. 21636722 2011
Entrez Id: 83478
Gene Symbol: ARHGAP24
ARHGAP24 		0.300 GermlineCausalMutation disease ORPHANET Arhgap24 inactivates Rac1 in mouse podocytes, and a mutant form is associated with familial focal segmental glomerulosclerosis. 21911940 2011
Entrez Id: 396
Gene Symbol: ARHGDIA
ARHGDIA 		0.300 GermlineCausalMutation disease ORPHANET ARHGDIA: a novel gene implicated in nephrotic syndrome. 23434736 2013
Entrez Id: 7827
Gene Symbol: NPHS2
NPHS2 		0.610 GeneticVariation disease CLINVAR Association between NPHS1 and NPHS2 gene variants and nephrotic syndrome in children. 25599733 2015