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PAX2 Gene Focal segmental glomerulosclerosis type 7 NGS Genetic Test

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PAX2 Gene Focal segmental glomerulosclerosis type 7 NGS Genetic Test

Short Name: PAX2 FSGS Type 7 NGS Test

Also known as: PAX2 Gene Test for FSGS, FSGS Type 7 Genetic Test, PAX2 Mutation Analysis

PAX2 Gene Focal segmental glomerulosclerosis type 7 NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses Next-Generation Sequencing (NGS) on Blood or Extracted DNA or One drop Blood on FTA Card samples. Results in 3 to 4 Weeks. Free home collection in 300+ cities across India.

NGS Genetic TestAll Ages🏠 Home Collection

🩺 Medically Reviewed By

Overview

The purpose of this test is to identify mutations in the PAX2 gene associated with Focal Segmental Glomerulosclerosis Type 7, enabling accurate diagnosis, genetic counseling, and personalized treatment strategies to manage kidney health and prevent complications.

Test Code
5393
Price
₹20,000
Sample Type
Blood or Extracted DNA or One drop Blood on FTA Card
Result Time
3 to 4 Weeks
Fasting Required
No
Method
Next-Generation Sequencing (NGS)
Step 1

Sample Collection

No specific preparation required. Provide clinical history and family pedigree during genetic counseling.

Method: Venipuncture or Finger Prick

Step 2

Laboratory Analysis

Blood sample collected via venipuncture or finger prick. Ensure proper labeling and handling.

Step 3

Report Delivery

Apply pressure to the puncture site. Store sample as instructed. Await report delivery.

Timeline: 3 to 4 Weeks

Patient Instructions

1
Before the Test:Undergo genetic counseling to understand implications. Provide detailed family medical history.
2
During the Test:Sample collection takes 10-15 minutes. Minimal discomfort from blood draw.
3
After the Test:Resume normal activities. Monitor puncture site for any issues. Await results via chosen delivery method.

About This Test

Who Should Get This Test

The purpose of this test is to identify mutations in the PAX2 gene associated with Focal Segmental Glomerulosclerosis Type 7, enabling accurate diagnosis, genetic counseling, and personalized treatment strategies to manage kidney health and prevent complications.

How to Prepare

  • Fast for 4-6 hours if specified, though not typically required
  • Avoid strenuous activity before collection
  • Bring identification and prescription
  • Inform about any medications or recent procedures

Doctor's Notes

Reviewed by — MBBS, MD (Medical Genetics) · Reg. No. 8532

"Early genetic testing for PAX2 mutations in suspected FSGS Type 7 can guide personalized treatment and family counseling, potentially slowing kidney disease progression."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Sample Volume3-5 mL
ContainerEDTA Tube or FTA Card
Collection MethodVenipuncture or Finger Prick

Sample Stability

Room Temperature24 hours
Refrigerated (2-8°C)72 hours
Frozen (-20°C)Long-term storage
Sample Rejection Criteria:
  • Hemolyzed or clotted sample
  • Insufficient sample volume
  • Incorrect container or labeling
  • Sample older than stability period

Understanding Your Results

Results indicate the presence or absence of mutations in the PAX2 gene. A positive result confirms genetic predisposition to FSGS Type 7, while a negative result suggests no detected mutations, but clinical correlation is essential.
📊

Positive for PAX2 mutation

Confirms diagnosis of FSGS Type 7. Recommend nephrology consultation, genetic counseling, and family screening.

📊

Negative for PAX2 mutation

No pathogenic mutation detected. Consider other causes of symptoms and further clinical evaluation.

📊

Variant of uncertain significance

Genetic variant found but clinical significance unknown. Requires follow-up testing and expert review.

⚠️ When to Consult a Doctor:

Consult a nephrologist or geneticist if symptoms persist, results are positive, or for family planning advice based on genetic findings.

Limitations

  • May not detect all genetic variants or mutations
  • Requires genetic counseling for interpretation
  • Results should be correlated with clinical findings
  • Limited to PAX2 gene analysis only

Risks & Considerations

  • Minor bruising or pain at puncture site
  • Rare risk of infection
  • Psychological impact of genetic results

Interfering Factors

  • Sample contamination
  • Degraded DNA quality
  • Incorrect sample storage
  • Recent blood transfusion

Compare With Similar Tests

TestPAX2 Gene Focal segmental glomerulosclerosis type 7 NGS Genetic Test
ComparisonPAX2 Gene Focal segmental glomerulosclerosis type 7 NGS Genetic TestInvasive but provides histological confirmation; genetic test is non-invasive and identifies root cause.Measures proteinuria symptomatically; genetic test detects underlying genetic mutation.Assesses kidney function; genetic test identifies specific genetic disorder.May cover multiple genes; this test is specific to PAX2 for FSGS Type 7.

Frequently Asked Questions

What is the PAX2 Gene FSGS Type 7 NGS Genetic Test?
It is a genetic test that uses Next-Generation Sequencing to detect mutations in the PAX2 gene, which cause Focal Segmental Glomerulosclerosis Type 7, a kidney disorder.
Who should take this test?
Individuals with symptoms like proteinuria, hematuria, edema, or a family history of FSGS or kidney disease should consider this test.
How is the test performed?
A blood sample or extracted DNA is collected and analyzed using NGS technology to sequence the PAX2 gene for mutations.
What is the cost of the test?
The test costs INR 20,000, which includes home sample collection across India.
Is fasting required before the test?
No, fasting is not typically required for this genetic test.
How long does it take to get results?
Results are usually available within 3 to 4 weeks after sample collection.
What do positive results mean?
A positive result confirms a mutation in the PAX2 gene, indicating a genetic predisposition to FSGS Type 7. Consult a nephrologist for management.
Are there any risks associated with the test?
Risks are minimal, such as slight bruising from blood draw. Genetic results may have psychological implications, so counseling is recommended.
Can this test be done at home?
Yes, DNA Labs India offers free home sample collection for this test across many cities in India.
What is the accuracy of the NGS Genetic Test?
NGS technology provides high accuracy in detecting mutations, but results should be interpreted alongside clinical findings.
Is genetic counseling included?
Yes, a genetic counseling session is recommended and often included to discuss results and family implications.
How do I book the test?
You can book online through DNA Labs India's website or contact their customer service for assistance.
Worried about the process? Our certified phlebotomists collect thousands of samples every month across India. The process takes under 5 minutes and is virtually painless. Questions? Message us on WhatsApp — we're here 7 days a week.

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