Condition: Proteinuria
rs1428826948
in
APOL1
gene and
Proteinuria
PMID 20647424
2010 Association of trypanolytic ApoL1 variants with kidney disease in African Americans.
rs74375025
in
CUBN
gene and
Proteinuria
PMID 30476138
2019 Sequence variants associating with urinary biomarkers.
rs2075252
in
LRP2
gene and
Proteinuria
PMID 30476138
2019 Sequence variants associating with urinary biomarkers.
rs869025495
in
NPHS2
gene and
Proteinuria
PMID 17899208
2007 NPHS2 (podicin) mutations in Turkish children with idiopathic nephrotic syndrome.
PMID 14675423
2004 Plasma membrane targeting of podocin through the classical exocytic pathway: effect of NPHS2 mutations.
PMID 15504144
2004 A novel NPHS2 gene mutation in Turkish children with familial steroid-resistant nephrotic syndrome.
PMID 14978175
2004 Patients with mutations in NPHS2 (podocin) do not respond to standard steroid treatment of nephrotic syndrome.
PMID 15253708
2004 NPHS2 mutation analysis shows genetic heterogeneity of steroid-resistant nephrotic syndrome and low post-transplant recurrence.