Gene: NPHS2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7827
Gene Symbol: NPHS2
NPHS2 		0.300 CausalMutation phenotype CLINVAR NPHS2 (podicin) mutations in Turkish children with idiopathic nephrotic syndrome. 17899208 2007
Entrez Id: 7827
Gene Symbol: NPHS2
NPHS2 		0.300 Biomarker phenotype RGD Nephrin and podocin dissociate at the onset of proteinuria in experimental membranous nephropathy. 15882266 2005
Entrez Id: 7827
Gene Symbol: NPHS2
NPHS2 		0.300 CausalMutation phenotype CLINVAR Plasma membrane targeting of podocin through the classical exocytic pathway: effect of NPHS2 mutations. 14675423 2004
Entrez Id: 7827
Gene Symbol: NPHS2
NPHS2 		0.300 CausalMutation phenotype CLINVAR A novel NPHS2 gene mutation in Turkish children with familial steroid-resistant nephrotic syndrome. 15504144 2004
Entrez Id: 7827
Gene Symbol: NPHS2
NPHS2 		0.300 CausalMutation phenotype 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 		0.300 CausalMutation phenotype 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 		0.300 GeneticVariation phenotype CLINVAR
Entrez Id: 7827
Gene Symbol: NPHS2
NPHS2 		0.300 Biomarker phenotype HPO