Nephrology
Renal Super Panel Broad
Overview
Test Name
Test Code
Test Category
Test Subcategory
Disease(s) Targeted
Who Is The Test For?
Test Approach
Whole exome sequencing (WES) with in silico gene panel analysis.
No. of Genes
Panel Content
Mitochondrial Genome Included In The Analysis
Deliverables
Clinical Report (Download a sample report here)
Turnaround Time
~3-6 weeks*
Specimen Requirements
For detailed information about the sample requirements, please consult our clinical sample requirements page.
About multiple kidney-related disorders
The Renal super panel includes most the genes from the different panels related to nephrological diseases.
If chosen, a well described phenotype is critical to ensure a proper variant interpretation.
The Renal Super Panel Broad is a comprehensive genetic test that screens for multiple kidney-related disorders to aid early diagnosis and guide treatment. These conditions are passed down through families and can lead to impaired kidney function, kidney failure, and other complications depending on the specific gene variant. Examples are the Autosomal Dominant Polycystic Kidney Disease (ADPKD) (the most common form) and Alport Syndrome. This comprehensive panel includes genes associated with the following nephrology disorders:
- Alport/Haematuria
- Atypical haemolytic uraemic syndrome
- Cystic kidney disease
- Extreme Early onset hypertension
- Hereditary systemic amyloidosis
- Membranoproliferative glomerulonephritis including C3 glomerulopathy
- Nephrocalcinosis or nephrolithiasis
- Proteinuric renal disease
- Renal ciliopathies
- CAKUT
- Renal tubulopathies
- Tubulointerstitial kidney disease
- Unexplained kidney failure in young people
One mitochondrial gene is also included on this panel, MT-TF, which has been associated with tubulointerstitial kidney disease in multiple individuals in the literature.
Gene Panel Workflow
Order a test using our clinical portal
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