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.
🩺 Medically Reviewed By
Dr SULOCHANA HEMCHANDRA HOLLA
Consultant Medical Geneticist · Reg: 8532
Last reviewed: September 7, 2026
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)
Sample Collection
Provide detailed clinical history and family history of PCD symptoms. Genetic counseling is recommended.
Method: Blood draw or saliva collection
Laboratory Analysis
A small sample of blood or saliva is collected by a trained phlebotomist.
Report Delivery
The sample is labeled and sent to the laboratory for analysis.
Timeline: 3 to 4 weeks from sample receipt
Patient Instructions
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 Dr SULOCHANA HEMCHANDRA HOLLA — 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 Stability
- Hemolyzed or clotted blood sample
- Insufficient sample volume
- Improperly labeled sample
Understanding Your Results
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.
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
| Test | DNAAF2 Gene Primary ciliary dyskinesia type 10 NGS Genetic Test | Other PCD Genetic Panels |
|---|---|---|
| Comparison | DNAAF2 Gene Primary ciliary dyskinesia type 10 NGS Genetic Test |
Frequently Asked Questions
What is primary ciliary dyskinesia type 10?
What are the symptoms of PCD type 10?
How is PCD type 10 diagnosed?
What does the DNAAF2 gene test involve?
How much does the DNAAF2 gene test cost?
Is home sample collection available for this test?
How long does it take to get the test results?
What sample is required for the test?
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₹20,000Reference Laboratory Services
We serve as a reference laboratory for hospitals and clinics across India. Send samples from your facility with same-day pickup, priority processing, and results delivered through our online portal. Competitive institutional pricing available.
Your Data Privacy
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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