rs763162233
|
Entrez Id: |
4868 |
Gene Symbol: |
NPHS1 |
NPHS1
|
Finnish congenital nephrotic syndrome
|
|
0.700 |
GeneticVariation |
UNIPROT |
Mutations in podocyte genes are a rare cause of primary FSGS associated with ESRD in adult patients.
|
22732337 |
2012 |
rs763162233
|
Entrez Id: |
4868 |
Gene Symbol: |
NPHS1 |
NPHS1
|
Finnish congenital nephrotic syndrome
|
|
0.700 |
GeneticVariation |
UNIPROT |
Nineteen novel NPHS1 mutations in a worldwide cohort of patients with congenital nephrotic syndrome (CNS).
|
20172850 |
2010 |
rs763162233
|
Entrez Id: |
4868 |
Gene Symbol: |
NPHS1 |
NPHS1
|
Finnish congenital nephrotic syndrome
|
|
0.700 |
GeneticVariation |
UNIPROT |
Structure of the gene for congenital nephrotic syndrome of the finnish type (NPHS1) and characterization of mutations.
|
9915943 |
1999 |
rs763162233
|
Entrez Id: |
4868 |
Gene Symbol: |
NPHS1 |
NPHS1
|
Finnish congenital nephrotic syndrome
|
|
0.700 |
GeneticVariation |
UNIPROT |
Mutation spectrum in the nephrin gene (NPHS1) in congenital nephrotic syndrome.
|
11317351 |
2001 |
rs763162233
|
Entrez Id: |
4868 |
Gene Symbol: |
NPHS1 |
NPHS1
|
Finnish congenital nephrotic syndrome
|
|
0.700 |
GeneticVariation |
UNIPROT |
NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described.
|
26560236 |
2016 |
rs763162233
|
Entrez Id: |
4868 |
Gene Symbol: |
NPHS1 |
NPHS1
|
Finnish congenital nephrotic syndrome
|
|
0.700 |
GeneticVariation |
UNIPROT |
Immunosuppression and renal outcome in congenital and pediatric steroid-resistant nephrotic syndrome.
|
20798252 |
2010 |
rs763162233
|
Entrez Id: |
4868 |
Gene Symbol: |
NPHS1 |
NPHS1
|
Finnish congenital nephrotic syndrome
|
|
0.700 |
GeneticVariation |
UNIPROT |
Thirteen novel NPHS1 mutations in a large cohort of children with congenital nephrotic syndrome.
|
18503012 |
2008 |
rs763162233
|
Entrez Id: |
4868 |
Gene Symbol: |
NPHS1 |
NPHS1
|
Finnish congenital nephrotic syndrome
|
|
0.700 |
GeneticVariation |
UNIPROT |
Positionally cloned gene for a novel glomerular protein--nephrin--is mutated in congenital nephrotic syndrome.
|
9660941 |
1998 |
rs762392183
|
Entrez Id: |
4868 |
Gene Symbol: |
NPHS1 |
NPHS1
|
Finnish congenital nephrotic syndrome
|
C |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs762392183
|
Entrez Id: |
4868 |
Gene Symbol: |
NPHS1 |
NPHS1
|
Finnish congenital nephrotic syndrome
|
C |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs762184939
|
Entrez Id: |
4868 |
Gene Symbol: |
NPHS1 |
NPHS1
|
Finnish congenital nephrotic syndrome
|
C |
0.700 |
CausalMutation |
CLINVAR |
Spectrum of mutations in Chinese children with steroid-resistant nephrotic syndrome.
|
28204945 |
2017 |
rs762184939
|
Entrez Id: |
4868 |
Gene Symbol: |
NPHS1 |
NPHS1
|
Finnish congenital nephrotic syndrome
|
C |
0.700 |
CausalMutation |
CLINVAR |
Genetic basis of congenital and infantile nephrotic syndromes.
|
22099579 |
2011 |
rs758432802
|
Entrez Id: |
4868 |
Gene Symbol: |
NPHS1 |
NPHS1
|
Finnish congenital nephrotic syndrome
|
C |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs756436580
|
Entrez Id: |
4868 |
Gene Symbol: |
NPHS1 |
NPHS1
|
Finnish congenital nephrotic syndrome
|
GT |
0.700 |
GeneticVariation |
CLINVAR |
Interaction with podocin facilitates nephrin signaling.
|
11562357 |
2001 |
rs756436580
|
Entrez Id: |
4868 |
Gene Symbol: |
NPHS1 |
NPHS1
|
Finnish congenital nephrotic syndrome
|
GT |
0.700 |
GeneticVariation |
CLINVAR |
Clinical utility of genetic testing in children and adults with steroid-resistant nephrotic syndrome.
|
21415313 |
2011 |
rs756436580
|
Entrez Id: |
4868 |
Gene Symbol: |
NPHS1 |
NPHS1
|
Finnish congenital nephrotic syndrome
|
GT |
0.700 |
GeneticVariation |
CLINVAR |
Thirteen novel NPHS1 mutations in a large cohort of children with congenital nephrotic syndrome.
|
18503012 |
2008 |
rs755763002
|
Entrez Id: |
4868 |
Gene Symbol: |
NPHS1 |
NPHS1
|
Finnish congenital nephrotic syndrome
|
G |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs753476209
|
Entrez Id: |
4868 |
Gene Symbol: |
NPHS1 |
NPHS1
|
Finnish congenital nephrotic syndrome
|
|
0.700 |
GeneticVariation |
UNIPROT |
Nephrin mutations can cause childhood-onset steroid-resistant nephrotic syndrome.
|
18614772 |
2008 |
rs753476209
|
Entrez Id: |
4868 |
Gene Symbol: |
NPHS1 |
NPHS1
|
Finnish congenital nephrotic syndrome
|
|
0.700 |
GeneticVariation |
UNIPROT |
Mutations in podocyte genes are a rare cause of primary FSGS associated with ESRD in adult patients.
|
22732337 |
2012 |
rs753476209
|
Entrez Id: |
4868 |
Gene Symbol: |
NPHS1 |
NPHS1
|
Finnish congenital nephrotic syndrome
|
|
0.700 |
GeneticVariation |
UNIPROT |
Nineteen novel NPHS1 mutations in a worldwide cohort of patients with congenital nephrotic syndrome (CNS).
|
20172850 |
2010 |
rs753476209
|
Entrez Id: |
4868 |
Gene Symbol: |
NPHS1 |
NPHS1
|
Finnish congenital nephrotic syndrome
|
|
0.700 |
GeneticVariation |
UNIPROT |
A spectrum of novel NPHS1 and NPHS2 gene mutations in pediatric nephrotic syndrome patients from Pakistan.
|
22565185 |
2012 |
rs753476209
|
Entrez Id: |
4868 |
Gene Symbol: |
NPHS1 |
NPHS1
|
Finnish congenital nephrotic syndrome
|
|
0.700 |
GeneticVariation |
UNIPROT |
Two novel NPHS1 mutations in a Chinese family with congenital nephrotic syndrome.
|
22009864 |
2011 |
rs753476209
|
Entrez Id: |
4868 |
Gene Symbol: |
NPHS1 |
NPHS1
|
Finnish congenital nephrotic syndrome
|
|
0.700 |
GeneticVariation |
UNIPROT |
Defective nephrin trafficking caused by missense mutations in the NPHS1 gene: insight into the mechanisms of congenital nephrotic syndrome.
|
11726550 |
2001 |
rs753476209
|
Entrez Id: |
4868 |
Gene Symbol: |
NPHS1 |
NPHS1
|
Finnish congenital nephrotic syndrome
|
|
0.700 |
GeneticVariation |
UNIPROT |
Novel mutation in the nephrin gene of a Japanese patient with congenital nephrotic syndrome of the Finnish type.
|
10652016 |
2000 |
rs753476209
|
Entrez Id: |
4868 |
Gene Symbol: |
NPHS1 |
NPHS1
|
Finnish congenital nephrotic syndrome
|
|
0.700 |
GeneticVariation |
UNIPROT |
NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described.
|
26560236 |
2016 |