×
Entrez Id:
4868
Gene Symbol:
NPHS1
NPHS1
0.800
GeneticVariation
disease
CLINVAR
A molecular genetic analysis of childhood nephrotic syndrome in a cohort of Saudi Arabian families.
23595123
2013
×
Entrez Id:
4868
Gene Symbol:
NPHS1
NPHS1
0.800
GeneticVariation
disease
CLINVAR
Congenital nephrotic syndrome with prolonged renal survival without renal replacement therapy.
23949594
2013
×
Entrez Id:
4868
Gene Symbol:
NPHS1
NPHS1
0.800
CausalMutation
disease
CLINVAR
Congenital nephrotic syndrome with prolonged renal survival without renal replacement therapy.
23949594
2013
×
Entrez Id:
4868
Gene Symbol:
NPHS1
NPHS1
0.800
GeneticVariation
disease
CLINVAR
NPHS1 gene mutations in children with Nephrotic Syndrome in northwest Iran.
24498843
2013
×
Entrez Id:
4868
Gene Symbol:
NPHS1
NPHS1
0.800
GeneticVariation
disease
CLINVAR
Nephrin missense mutations: induction of endoplasmic reticulum stress and cell surface rescue by reduction in chaperone interactions.
24303155
2013
×
Entrez Id:
4868
Gene Symbol:
NPHS1
NPHS1
0.800
GeneticVariation
disease
CLINVAR
Mutations in podocyte genes are a rare cause of primary FSGS associated with ESRD in adult patients.
22732337
2012
×
Entrez Id:
4868
Gene Symbol:
NPHS1
NPHS1
0.800
GeneticVariation
disease
CLINVAR
Rituximab treatment for recurrence of nephrotic syndrome in a pediatric patient after renal transplantation for congenital nephrotic syndrome of Finnish type.
21672106
2012
×
Entrez Id:
4868
Gene Symbol:
NPHS1
NPHS1
0.800
GeneticVariation
disease
CLINVAR
Mutation analysis of NPHS1 in a worldwide cohort of congenital nephrotic syndrome patients.
22584503
2012
×
Entrez Id:
4868
Gene Symbol:
NPHS1
NPHS1
0.800
GeneticVariation
disease
UNIPROT
A spectrum of novel NPHS1 and NPHS2 gene mutations in pediatric nephrotic syndrome patients from Pakistan.
22565185
2012
×
Entrez Id:
4868
Gene Symbol:
NPHS1
NPHS1
0.800
GeneticVariation
disease
UNIPROT
Mutations in podocyte genes are a rare cause of primary FSGS associated with ESRD in adult patients.
22732337
2012
×
Entrez Id:
4868
Gene Symbol:
NPHS1
NPHS1
0.800
CausalMutation
disease
CLINVAR
A spectrum of novel NPHS1 and NPHS2 gene mutations in pediatric nephrotic syndrome patients from Pakistan.
22565185
2012
×
Entrez Id:
4868
Gene Symbol:
NPHS1
NPHS1
0.800
GeneticVariation
disease
CLINVAR
Two novel NPHS1 mutations in a Chinese family with congenital nephrotic syndrome.
22009864
2011
×
Entrez Id:
4868
Gene Symbol:
NPHS1
NPHS1
0.800
CausalMutation
disease
CLINVAR
Genetic basis of congenital and infantile nephrotic syndromes.
22099579
2011
×
Entrez Id:
4868
Gene Symbol:
NPHS1
NPHS1
0.800
GeneticVariation
disease
UNIPROT
Two novel NPHS1 mutations in a Chinese family with congenital nephrotic syndrome.
22009864
2011
×
Entrez Id:
4868
Gene Symbol:
NPHS1
NPHS1
0.800
GeneticVariation
disease
CLINVAR
Clinical utility of genetic testing in children and adults with steroid-resistant nephrotic syndrome.
21415313
2011
×
Entrez Id:
4868
Gene Symbol:
NPHS1
NPHS1
0.800
CausalMutation
disease
CLINVAR
Clinical utility of genetic testing in children and adults with steroid-resistant nephrotic syndrome.
21415313
2011
×
Entrez Id:
4868
Gene Symbol:
NPHS1
NPHS1
0.800
GeneticVariation
disease
UNIPROT
Nineteen novel NPHS1 mutations in a worldwide cohort of patients with congenital nephrotic syndrome (CNS).
20172850
2010
×
Entrez Id:
4868
Gene Symbol:
NPHS1
NPHS1
0.800
CausalMutation
disease
CLINVAR
Genotype-phenotype correlations in non-Finnish congenital nephrotic syndrome.
20507940
2010
×
Entrez Id:
4868
Gene Symbol:
NPHS1
NPHS1
0.800
GeneticVariation
disease
CLINVAR
Genotype-phenotype correlations in non-Finnish congenital nephrotic syndrome.
20507940
2010
×
Entrez Id:
4868
Gene Symbol:
NPHS1
NPHS1
0.800
GeneticVariation
disease
CLINVAR
Nineteen novel NPHS1 mutations in a worldwide cohort of patients with congenital nephrotic syndrome (CNS).
20172850
2010
×
Entrez Id:
4868
Gene Symbol:
NPHS1
NPHS1
0.800
GeneticVariation
disease
UNIPROT
Immunosuppression and renal outcome in congenital and pediatric steroid-resistant nephrotic syndrome.
20798252
2010
×
Entrez Id:
4868
Gene Symbol:
NPHS1
NPHS1
0.800
GeneticVariation
disease
BEFREE
A subgroup of NTEC known as NTEC-2 produce a variant of CNF (CNF-2 ) whose gene is located on a plasmid known as Vir.
20060660
2010
×
Entrez Id:
4868
Gene Symbol:
NPHS1
NPHS1
0.800
CausalMutation
disease
CLINVAR
Immunosuppression and renal outcome in congenital and pediatric steroid-resistant nephrotic syndrome.
20798252
2010
×
Entrez Id:
4868
Gene Symbol:
NPHS1
NPHS1
0.800
CausalMutation
disease
CLINVAR
Nineteen novel NPHS1 mutations in a worldwide cohort of patients with congenital nephrotic syndrome (CNS).
20172850
2010
×
Entrez Id:
4868
Gene Symbol:
NPHS1
NPHS1
0.800
GeneticVariation
disease
CLINVAR
Nephrin mutations cause childhood- and adult-onset focal segmental glomerulosclerosis.
19812541
2009