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DNAI2 Gene Primary ciliary dyskinesia type 9 NGS Genetic Test

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DNAI2 Gene Primary ciliary dyskinesia type 9 NGS Genetic Test

Short Name: DNAI2 PCD Type 9 NGS Test

Also known as: PCD Type 9, DNAI2-related primary ciliary dyskinesia

DNAI2 Gene Primary ciliary dyskinesia type 9 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 Test🏠 Home Collection

🩺 Medically Reviewed By

Overview

To identify pathogenic mutations in the DNAI2 gene for the diagnosis of primary ciliary dyskinesia type 9, enabling early intervention and family genetic counseling.

Test Code
4788
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 if available.

Method: Venipuncture or finger-prick

Step 2

Laboratory Analysis

Blood sample collected via venipuncture or finger-prick onto FTA card.

Step 3

Report Delivery

Apply pressure to the puncture site. Store sample as per instructions.

Timeline: 3 to 4 Weeks

Patient Instructions

1
Before the Test:Provide informed consent and clinical history. No fasting required.
2
During the Test:Sample collection takes a few minutes with minimal discomfort.
3
After the Test:Resume normal activities. Await report in 3-4 weeks.

About This Test

Who Should Get This Test

To identify pathogenic mutations in the DNAI2 gene for the diagnosis of primary ciliary dyskinesia type 9, enabling early intervention and family genetic counseling.

How to Prepare

  • Ensure proper labeling of sample
  • Use sterile equipment
  • Transport sample at ambient temperature

Doctor's Notes

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

"Early genetic diagnosis of primary ciliary dyskinesia type 9 through NGS testing can guide personalized management, prevent complications, and improve quality of life for patients."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Sample VolumeAs required for NGS analysis
ContainerEDTA tube or FTA card
Collection MethodVenipuncture or finger-prick

Sample Stability

Blood: 7 days at room temperature
FTA card: Stable for months if stored properly
Sample Rejection Criteria:
  • Hemolyzed sample
  • Insufficient sample volume
  • Incorrect container

Understanding Your Results

Results indicate the presence or absence of mutations in the DNAI2 gene. A positive result confirms diagnosis of PCD type 9, while a negative result may require further testing.
📊

Pathogenic variant detected

Confirms diagnosis of DNAI2 gene PCD type 9. Genetic counseling recommended.

📊

No pathogenic variant detected

PCD type 9 unlikely, but clinical correlation and additional tests may be needed.

📊

Variant of uncertain significance

Further family studies or functional analysis required.

⚠️ When to Consult a Doctor:

Consult a genetic specialist or pulmonologist if symptoms persist or if family history suggests PCD.

Limitations

  • NGS may not detect all types of mutations, such as large deletions or duplications
  • Results require interpretation by a genetic specialist
  • Test does not cover other PCD-related genes

Risks & Considerations

  • Minor bruising at puncture site
  • Rare infection risk

Interfering Factors

  • Sample contamination
  • Degraded DNA
  • Incorrect sample storage

Frequently Asked Questions

What is the DNAI2 Gene Primary Ciliary Dyskinesia Type 9 NGS Genetic Test?
It is a genetic test using next-generation sequencing to detect mutations in the DNAI2 gene, which causes primary ciliary dyskinesia type 9.
What are the symptoms of DNAI2 gene PCD type 9?
Symptoms include chronic cough, nasal congestion, sinusitis, bronchitis, recurrent pneumonia, ear infections, and hearing loss.
How is the test performed?
A blood sample or DNA extract is analyzed using NGS technology to identify mutations in the DNAI2 gene.
What is the cost of this test in India?
The cost is INR 20,000, with free home sample collection available across India.
Is fasting required for this test?
No, fasting is not required.
How long does it take to get results?
Results are typically available in 3 to 4 weeks.
Is home sample collection available?
Yes, free home collection is offered for online bookings in many cities across India.
What does a positive result mean?
A positive result confirms a diagnosis of DNAI2 gene PCD type 9, guiding management and genetic counseling.
Can this test detect all mutations in the DNAI2 gene?
NGS is highly accurate but may not detect all mutation types, such as large structural variants.
Who should consider this test?
Individuals with chronic respiratory symptoms, recurrent infections, or a family history of PCD.
Is genetic counseling recommended?
Yes, genetic counseling is advised before and after testing to discuss implications and family planning.
What are the risks of the test?
Risks are minimal, including minor bruising from blood draw. No significant health risks are associated with the test itself.
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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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.

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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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