TRPC6 - focal segmental glomerulosclerosis type 2

This test is available for the following conditions:

  • Conditions > Renal / Nephrological > Nephrotic syndrome

This product is also part of the following panels:

  • Mendelian inherited disorders panel with genome wide CNV analysis
  • Renal disorders panel

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries

OMIM: 603652
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 435

Gene

ACTN4 - nephrotic syndrome with focal segmental glomerular sclerosis

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 484

ACTN4 - nephrotic syndrome with focal segmental glomerular sclerosis



€ 484

ACTN4 - nephrotic syndrome with focal segmental glomerular sclerosis

This test is available for the following conditions:

  • Conditions > Renal / Nephrological > Nephrotic syndrome

This product is also part of the following panels:

  • Mendelian inherited disorders panel with genome wide CNV analysis
  • Renal disorders panel

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries

OMIM: 604638
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 484
Gene

CD2AP - focal segmental glomerulosclerosis type 3

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 468

CD2AP - focal segmental glomerulosclerosis type 3



€ 468

CD2AP - focal segmental glomerulosclerosis type 3

This test is available for the following conditions:

  • Conditions > Renal / Nephrological > Nephrotic syndrome

This product is also part of the following panels:

  • Comprehensive preconception carrier test panel¹
  • Mendelian inherited disorders panel with genome wide CNV analysis
  • Renal disorders panel

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries

OMIM: 604241
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 468
Gene

INF2 - focal segmental glomerulosclerosis type 5

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 476

INF2 - focal segmental glomerulosclerosis type 5



€ 476

INF2 - focal segmental glomerulosclerosis type 5

This test is available for the following conditions:

  • Conditions > Renal / Nephrological > Nephrotic syndrome

This product is also part of the following panels:

  • Mendelian inherited disorders panel with genome wide CNV analysis
  • Neuropathies panel¹
  • Renal disorders panel

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries
Remarks
Exon 8 is technically impossible to analyze.

OMIM: 610982
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 476
Gene

LAMB2 - congenital nephrotic syndrome (Pierson syndrome)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 476

LAMB2 - congenital nephrotic syndrome (Pierson syndrome)



€ 476

LAMB2 - congenital nephrotic syndrome (Pierson syndrome)

This test is available for the following conditions:

  • Conditions > Renal / Nephrological > Nephrotic syndrome

This product is also part of the following panels:

  • Comprehensive preconception carrier test panel¹
  • Intellectual disability panel with genome wide CNV analysis
  • Mendelian inherited disorders panel with genome wide CNV analysis
  • Renal disorders panel
  • Vision disorders panel

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries

OMIM: 150325
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 476
Gene

MYO1E - focal segmental glomerulosclerosis type 6

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 542

MYO1E - focal segmental glomerulosclerosis type 6



€ 542

MYO1E - focal segmental glomerulosclerosis type 6

This test is available for the following conditions:

  • Conditions > Renal / Nephrological > Nephrotic syndrome

This product is also part of the following panels:

  • Comprehensive preconception carrier test panel¹
  • Mendelian inherited disorders panel with genome wide CNV analysis
  • Renal disorders panel

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries

OMIM: 601479
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 542
Gene

NPHS1 - congenital nephrotic syndrome of the Finnish type

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 492

NPHS1 - congenital nephrotic syndrome of the Finnish type



€ 492

NPHS1 - congenital nephrotic syndrome of the Finnish type

This test is available for the following conditions:

  • Conditions > Renal / Nephrological > Nephrotic syndrome

This product is also part of the following panels:

  • Comprehensive preconception carrier test panel¹
  • Mendelian inherited disorders panel with genome wide CNV analysis
  • Renal disorders panel

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries

OMIM: 602716
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 492
Gene

NPHS2 - steroid-resistant nephrotic syndrome

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 377

NPHS2 - steroid-resistant nephrotic syndrome



€ 377

NPHS2 - steroid-resistant nephrotic syndrome

This test is available for the following conditions:

  • Conditions > Renal / Nephrological > Nephrotic syndrome

This product is also part of the following panels:

  • Comprehensive preconception carrier test panel¹
  • Mendelian inherited disorders panel with genome wide CNV analysis
  • Renal disorders panel

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries

OMIM: 604766
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 377
Gene

PAX2 - focal segmental glomurulosclerosis type 7

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 402

PAX2 - focal segmental glomurulosclerosis type 7



€ 402

PAX2 - focal segmental glomurulosclerosis type 7

This test is available for the following conditions:

  • Conditions > Renal / Nephrological > Nephrotic syndrome

This product is also part of the following panels:

  • Mendelian inherited disorders panel with genome wide CNV analysis
  • Renal disorders panel
  • Vision disorders panel

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries

OMIM: 22967
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 402
Gene

PLCE1 - nephrotic syndrome type 3

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 591

PLCE1 - nephrotic syndrome type 3



€ 591

PLCE1 - nephrotic syndrome type 3

This test is available for the following conditions:

  • Conditions > Renal / Nephrological > Nephrotic syndrome

This product is also part of the following panels:

  • Comprehensive preconception carrier test panel¹
  • Mendelian inherited disorders panel with genome wide CNV analysis
  • Metabolic disorders panel
  • Renal disorders panel

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries

OMIM: 608414
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 591
Gene

PTPRO - nephrotic syndrome type 6

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 583

PTPRO - nephrotic syndrome type 6



€ 583

PTPRO - nephrotic syndrome type 6

This test is available for the following conditions:

  • Conditions > Renal / Nephrological > Nephrotic syndrome

This product is also part of the following panels:

  • Comprehensive preconception carrier test panel¹
  • Mendelian inherited disorders panel with genome wide CNV analysis
  • Renal disorders panel

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries

OMIM: 600579
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 583
Gene

TRPC6 - focal segmental glomerulosclerosis type 2

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 435

TRPC6 - focal segmental glomerulosclerosis type 2



€ 435
Gene

WT1 - nephrotic syndrome with diffuse mesangial sclerosis

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 393

WT1 - nephrotic syndrome with diffuse mesangial sclerosis



€ 393

WT1 - nephrotic syndrome with diffuse mesangial sclerosis

This test is available for the following conditions:

  • Conditions > Renal / Nephrological > Nephrotic syndrome

This product is also part of the following panels:

  • Disorders/differences of sex development (DSD) / Primary adrenal insufficiency panel
  • Hereditary cancer panel
  • Mendelian inherited disorders panel with genome wide CNV analysis
  • Renal disorders panel

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries

OMIM: 256370
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 393