Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7827
Gene Symbol: NPHS2
NPHS2 		0.610 GeneticVariation disease CLINVAR Patients with mutations in NPHS2 (podocin) do not respond to standard steroid treatment of nephrotic syndrome. 14978175 2004
Entrez Id: 7827
Gene Symbol: NPHS2
NPHS2 		0.610 CausalMutation disease CLINVAR In vivo expression of podocyte slit diaphragm-associated proteins in nephrotic patients with NPHS2 mutation. 15327385 2004
Entrez Id: 7827
Gene Symbol: NPHS2
NPHS2 		0.610 CausalMutation disease CLINVAR Disease-causing missense mutations in NPHS2 gene alter normal nephrin trafficking to the plasma membrane. 15496146 2004
Entrez Id: 7827
Gene Symbol: NPHS2
NPHS2 		0.610 CausalMutation disease CLINVAR Patients with mutations in NPHS2 (podocin) do not respond to standard steroid treatment of nephrotic syndrome. 14978175 2004
Entrez Id: 7827
Gene Symbol: NPHS2
NPHS2 		0.610 CausalMutation disease CLINVAR NPHS2 mutation associated with recurrence of proteinuria after transplantation. 15015071 2004
Entrez Id: 7827
Gene Symbol: NPHS2
NPHS2 		0.610 GeneticVariation disease CLINVAR Disease-causing missense mutations in NPHS2 gene alter normal nephrin trafficking to the plasma membrane. 15496146 2004
Entrez Id: 7827
Gene Symbol: NPHS2
NPHS2 		0.610 GeneticVariation disease CLINVAR Plasma membrane targeting of podocin through the classical exocytic pathway: effect of NPHS2 mutations. 14675423 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: 7827
Gene Symbol: NPHS2
NPHS2 		0.610 GeneticVariation disease CLINVAR In vivo expression of podocyte slit diaphragm-associated proteins in nephrotic patients with NPHS2 mutation. 15327385 2004
Entrez Id: 7827
Gene Symbol: NPHS2
NPHS2 		0.610 CausalMutation disease CLINVAR NPHS2 mutation analysis shows genetic heterogeneity of steroid-resistant nephrotic syndrome and low post-transplant recurrence. 15253708 2004
Entrez Id: 7827
Gene Symbol: NPHS2
NPHS2 		0.610 GeneticVariation disease CLINVAR NPHS2 mutation analysis shows genetic heterogeneity of steroid-resistant nephrotic syndrome and low post-transplant recurrence. 15253708 2004
Entrez Id: 4868
Gene Symbol: NPHS1
NPHS1 		0.400 GeneticVariation disease CLINVAR Nephrin gene (NPHS1) in patients with minimal change nephrotic syndrome (MCNS). 15086927 2004
Entrez Id: 126859
Gene Symbol: AXDND1
AXDND1 		0.100 CausalMutation disease CLINVAR Patients with mutations in NPHS2 (podocin) do not respond to standard steroid treatment of nephrotic syndrome. 14978175 2004
Entrez Id: 126859
Gene Symbol: AXDND1
AXDND1 		0.100 GeneticVariation disease CLINVAR Disease-causing missense mutations in NPHS2 gene alter normal nephrin trafficking to the plasma membrane. 15496146 2004
Entrez Id: 126859
Gene Symbol: AXDND1
AXDND1 		0.100 GeneticVariation disease CLINVAR Patients with mutations in NPHS2 (podocin) do not respond to standard steroid treatment of nephrotic syndrome. 14978175 2004
Entrez Id: 126859
Gene Symbol: AXDND1
AXDND1 		0.100 CausalMutation disease CLINVAR NPHS2 mutation associated with recurrence of proteinuria after transplantation. 15015071 2004
Entrez Id: 126859
Gene Symbol: AXDND1
AXDND1 		0.100 GeneticVariation disease CLINVAR NPHS2 mutation analysis shows genetic heterogeneity of steroid-resistant nephrotic syndrome and low post-transplant recurrence. 15253708 2004
Entrez Id: 126859
Gene Symbol: AXDND1
AXDND1 		0.100 CausalMutation disease CLINVAR In vivo expression of podocyte slit diaphragm-associated proteins in nephrotic patients with NPHS2 mutation. 15327385 2004
Entrez Id: 126859
Gene Symbol: AXDND1
AXDND1 		0.100 CausalMutation disease CLINVAR Plasma membrane targeting of podocin through the classical exocytic pathway: effect of NPHS2 mutations. 14675423 2004
Entrez Id: 126859
Gene Symbol: AXDND1
AXDND1 		0.100 GeneticVariation disease CLINVAR In vivo expression of podocyte slit diaphragm-associated proteins in nephrotic patients with NPHS2 mutation. 15327385 2004
Entrez Id: 126859
Gene Symbol: AXDND1
AXDND1 		0.100 CausalMutation disease CLINVAR NPHS2 mutation analysis shows genetic heterogeneity of steroid-resistant nephrotic syndrome and low post-transplant recurrence. 15253708 2004
Entrez Id: 126859
Gene Symbol: AXDND1
AXDND1 		0.100 GeneticVariation disease CLINVAR Plasma membrane targeting of podocin through the classical exocytic pathway: effect of NPHS2 mutations. 14675423 2004
Entrez Id: 7827
Gene Symbol: NPHS2
NPHS2 		0.610 GeneticVariation disease CLINVAR Mutations in NPHS2 in sporadic steroid-resistant nephrotic syndrome in Chinese children. 15769810 2005
Entrez Id: 7827
Gene Symbol: NPHS2
NPHS2 		0.610 GeneticVariation disease CLINVAR NPHS2 (Podocin) mutations in nephrotic syndrome. Clinical spectrum and fine mechanisms. 15817495 2005
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