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DNAAF2 Gene Primary ciliary dyskinesia type 10 NGS Genetic Test

DNA Labs India | ISO 9001:2015 Certified

DNAAF2 Gene Primary ciliary dyskinesia type 10 NGS Genetic Test

Also known as: PCD Type 10 Genetic Test, DNAAF2 Mutation Analysis

DNAAF2 Gene Primary ciliary dyskinesia type 10 NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses NGS (Next-Generation Sequencing) on Blood or Extracted DNA or One drop Blood on FTA Card samples. Results in 3 to 4 weeks from sample receipt. Free home collection in 300+ cities across India.

NGS Genetic Test🏠 Home Collection

🩺 Medically Reviewed By

Overview

To detect mutations in the DNAAF2 gene for diagnosis of primary ciliary dyskinesia type 10.

Test Code
4766
Price
₹20,000
Sample Type
Blood or Extracted DNA or One drop Blood on FTA Card
Result Time
3 to 4 weeks from sample receipt
Fasting Required
No
Method
NGS (Next-Generation Sequencing)
Step 1

Sample Collection

Provide detailed clinical history and family history of PCD symptoms. Genetic counseling is recommended.

Method: Blood draw or saliva collection

Step 2

Laboratory Analysis

A small sample of blood or saliva is collected by a trained phlebotomist.

Step 3

Report Delivery

The sample is labeled and sent to the laboratory for analysis.

Timeline: 3 to 4 weeks from sample receipt

Patient Instructions

1
Before the Test:Genetic counseling to discuss implications of testing and family history.
2
During the Test:Sample collection and processing in the laboratory.
3
After the Test:Report generation and consultation with a geneticist or physician.

About This Test

Who Should Get This Test

To detect mutations in the DNAAF2 gene for diagnosis of primary ciliary dyskinesia type 10.

How to Prepare

  • No fasting required
  • Ensure sample is not contaminated
  • Follow instructions for FTA card if used

Doctor's Notes

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

"Genetic testing for PCD Type 10 is essential for accurate diagnosis. Early detection can guide management and improve patient outcomes."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Sample VolumeAs per requirement
Collection MethodBlood draw or saliva collection

Sample Stability

Blood: Stable for 24 hours at room temperature
Extracted DNA: Stable for extended periods when stored properly
Sample Rejection Criteria:
  • Hemolyzed or clotted blood sample
  • Insufficient sample volume
  • Improperly labeled sample

Understanding Your Results

Results indicate whether pathogenic mutations in the DNAAF2 gene are detected.
📊

Positive for pathogenic mutation

Confirms diagnosis of PCD type 10. Genetic counseling and management recommended.

📊

Negative for pathogenic mutation

PCD type 10 is unlikely based on this gene. Clinical evaluation and other tests may be needed.

⚠️ When to Consult a Doctor:

If you experience symptoms of PCD such as chronic respiratory infections, sinusitis, or infertility, or if there is a family history of PCD.

Limitations

  • May not detect all genetic variants
  • Requires clinical correlation and genetic counseling

Risks & Considerations

  • Minimal risk from blood draw (bruising, infection)
  • Potential psychological impact of genetic results

Interfering Factors

  • Sample contamination
  • Degraded DNA

Compare With Similar Tests

TestDNAAF2 Gene Primary ciliary dyskinesia type 10 NGS Genetic TestOther PCD Genetic Panels
ComparisonDNAAF2 Gene Primary ciliary dyskinesia type 10 NGS Genetic Test

Frequently Asked Questions

What is primary ciliary dyskinesia type 10?
PCD type 10 is a rare genetic disorder caused by mutations in the DNAAF2 gene, leading to dysfunction of cilia and symptoms like chronic respiratory infections.
What are the symptoms of PCD type 10?
Symptoms include chronic respiratory infections, sinusitis, chronic cough, shortness of breath, frequent ear infections, and infertility.
How is PCD type 10 diagnosed?
Diagnosis is confirmed through genetic testing, such as the DNAAF2 Gene NGS Genetic Test, which detects mutations in the DNAAF2 gene.
What does the DNAAF2 gene test involve?
The test involves collecting a blood or saliva sample and analyzing it using next-generation sequencing to identify mutations in the DNAAF2 gene.
How much does the DNAAF2 gene test cost?
The cost is INR 20,000 at DNA Labs India, with home sample collection available.
Is home sample collection available for this test?
Yes, DNA Labs India offers free home sample collection across India for this test.
How long does it take to get the test results?
Results are typically available within 3 to 4 weeks after sample collection.
What sample is required for the test?
A blood sample, extracted DNA, or one drop of blood on an FTA card can be used.
Is fasting required before the test?
No, fasting is not required for this genetic test.
Who should consider getting this test?
Individuals with symptoms of PCD or a family history of PCD should consider this test after consulting a doctor.
What if the test result is positive?
A positive result confirms PCD type 10, and genetic counseling along with management strategies should be discussed with a healthcare provider.
Is the test covered by insurance?
Coverage depends on the insurance policy. It is advisable to check with your insurance provider.
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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Your medical data is protected under Indian law.

Stored in India: All patient records are stored on servers located in India. No data is transferred outside the country.

DPDP Act Compliant: Under the Digital Personal Data Protection Act 2023, you can request deletion of your records at any time by contacting support.

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