Nephrotic Syndrome, Type 10; Nphs10

Table of contents:

Description
Related genes
Clinical Features
Incidence and onset information
Alternative Names
Researches and researchers
Gene Panels
Sources and references

Genes related to Nephrotic Syndrome, Type 10; Nphs10

EMP2

View recommended genes panels

Clinical Features

Phenotypes and symptoms related to Nephrotic Syndrome, Type 10; Nphs10

Abnormality of the kidney
Nephrotic syndrome
Steroid-resistant nephrotic syndrome
Minimal change glomerulonephritis
Podocyte foot process effacement

Incidence and onset information

— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
— The onset for some of the known clinical features related to this disease may vary, including childhood onset, childhood onset, and childhood onset .

Researches and researchers

Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.

Nephrotic Syndrome, Type 10; Nphs10 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Nephrotic syndrome (NGS panel for 11 genes). By CGC Genetics (Portugal). WT1, NPHS2, ACTN4, PLCE1, COQ8B, DGKE, EMP2, LAMB2, ARHGDIA, NPHS1, PTPRO Specificity 10 % Genes 100 %
Nephrotic Syndrome (sequence analyis of EMP2 gene). By CGC Genetics (Portugal). EMP2 Specificity 100 % Genes 100 %
Nephrotic Syndrome (sequence analyis of EMP2 gene). By CGC Genetics (Portugal). EMP2 Specificity 100 % Genes 100 %
Nephrotic Syndrome (NS)/Focal Segmental Glomerulosclerosis (FSGS) Sequencing Panel with CNV Detection. By PreventionGenetics PreventionGenetics (United States). SGPL1, SMARCAL1, TRPC6, WT1, NPHS2, ANLN, CD2AP, TP53RK, ACTN4, SCARB2, PLCE1, XPO5, OSGEP, NUP205, CRB2, MAGI2, COQ8B, KANK1, COQ6, COL4A3 , (...) View the complete list with 29 more genes Panel complete gene list SGPL1, SMARCAL1, TRPC6, WT1, NPHS2, ANLN, CD2AP, TP53RK, ACTN4, SCARB2, PLCE1, XPO5, OSGEP, NUP205, CRB2, MAGI2, COQ8B, KANK1, COQ6, COL4A3, COL4A4, COL4A5, COL4A6, PDSS2, INF2, TPRKB, COQ2, ARHGAP24, CUBN, TTC21B, WDR73, LAGE3, KANK4, DGKE, NUP93, KANK2, NUP107, EMP2, FAT1, ITGA3, ITGB4, LAMA5, LAMB2, LMX1B, ARHGDIA, MYO1E, NPHS1, PAX2, PTPRO Specificity 3 % Genes 100 %
Nephrotic Syndrome via EMP2 Gene Sequencing with CNV Detection. By PreventionGenetics PreventionGenetics (United States). EMP2 Specificity 100 % Genes 100 %
Nephrotic syndrome and related disorders Comprehensive panel. By Connective Tissue Gene Tests (United States). SGPL1, SMARCAL1, TRPC6, WT1, NPHS2, ANLN, CD2AP, ACTN4, SCARB2, PLCE1, NUP205, CRB2, MAGI2, COQ8B, COQ6, COL4A3, COL4A4, COL4A5, COL4A6, PDSS2 , (...) View the complete list with 22 more genes Panel complete gene list SGPL1, SMARCAL1, TRPC6, WT1, NPHS2, ANLN, CD2AP, ACTN4, SCARB2, PLCE1, NUP205, CRB2, MAGI2, COQ8B, COQ6, COL4A3, COL4A4, COL4A5, COL4A6, PDSS2, INF2, COQ2, ARHGAP24, CUBN, TTC21B, WDR73, DGKE, NUP93, KANK2, NUP107, EMP2, FN1, ITGA3, ITGB4, LAMB2, LMX1B, ARHGDIA, MEFV, MYO1E, NPHS1, PAX2, PTPRO Specificity 3 % Genes 100 %
Nephrotic syndrome and related disorders NGS panel. By Connective Tissue Gene Tests (United States). SGPL1, SMARCAL1, TRPC6, WT1, NPHS2, ANLN, CD2AP, ACTN4, SCARB2, PLCE1, NUP205, CRB2, MAGI2, COQ8B, COQ6, COL4A3, COL4A4, COL4A5, COL4A6, PDSS2 , (...) View the complete list with 22 more genes Panel complete gene list SGPL1, SMARCAL1, TRPC6, WT1, NPHS2, ANLN, CD2AP, ACTN4, SCARB2, PLCE1, NUP205, CRB2, MAGI2, COQ8B, COQ6, COL4A3, COL4A4, COL4A5, COL4A6, PDSS2, INF2, COQ2, ARHGAP24, CUBN, TTC21B, WDR73, DGKE, NUP93, KANK2, NUP107, EMP2, FN1, ITGA3, ITGB4, LAMB2, LMX1B, ARHGDIA, MEFV, MYO1E, NPHS1, PAX2, PTPRO Specificity 3 % Genes 100 %
Nephrotic syndrome and related disorders Deletion / Duplication panel. By Connective Tissue Gene Tests (United States). SGPL1, SMARCAL1, TRPC6, WT1, NPHS2, ANLN, CD2AP, ACTN4, SCARB2, PLCE1, NUP205, CRB2, MAGI2, COQ8B, COQ6, COL4A3, COL4A4, COL4A5, COL4A6, PDSS2 , (...) View the complete list with 22 more genes Panel complete gene list SGPL1, SMARCAL1, TRPC6, WT1, NPHS2, ANLN, CD2AP, ACTN4, SCARB2, PLCE1, NUP205, CRB2, MAGI2, COQ8B, COQ6, COL4A3, COL4A4, COL4A5, COL4A6, PDSS2, INF2, COQ2, ARHGAP24, CUBN, TTC21B, WDR73, DGKE, NUP93, KANK2, NUP107, EMP2, FN1, ITGA3, ITGB4, LAMB2, LMX1B, ARHGDIA, MEFV, MYO1E, NPHS1, PAX2, PTPRO Specificity 3 % Genes 100 %

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Sources and references

You can check the following sources for additional information.

OMIM Rare Disease Symptoms Checker

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