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CCDC39 Gene Primary ciliary dyskinesia type 14 NGS Genetic Test

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CCDC39 Gene Primary ciliary dyskinesia type 14 NGS Genetic Test

Short Name: CCDC39 Gene PCD Type 14 NGS Test

Also known as: PCD Type 14, CCDC39-related Primary Ciliary Dyskinesia

CCDC39 Gene Primary ciliary dyskinesia type 14 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 TestAll Ages🏠 Home Collection

🩺 Medically Reviewed By

Overview

To identify pathogenic mutations in the CCDC39 gene for the diagnosis of Primary Ciliary Dyskinesia Type 14.

Test Code
4769
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

A genetic counseling session is recommended to discuss the test and implications.

Method: Venipuncture or Finger prick

Step 2

Laboratory Analysis

A blood sample is collected via venipuncture or a drop on FTA card.

Step 3

Report Delivery

The sample is processed and analyzed in the laboratory.

Timeline: 3 to 4 weeks from sample receipt

Patient Instructions

1
Before the Test:Genetic counseling and clinical history review.
2
During the Test:Sample collection procedure.
3
After the Test:Report generation and follow-up consultation.

About This Test

Who Should Get This Test

To identify pathogenic mutations in the CCDC39 gene for the diagnosis of Primary Ciliary Dyskinesia Type 14.

How to Prepare

  • Ensure proper patient identification
  • Avoid hemolysis during blood draw
  • Label samples correctly

Doctor's Notes

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

"Genetic testing for CCDC39 gene is essential for confirming PCD Type 14 diagnosis and informing treatment strategies."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Sample VolumeAs required
ContainerEDTA tube or FTA card
Collection MethodVenipuncture or Finger prick

Sample Stability

Sample Rejection Criteria:
  • Insufficient sample volume
  • Improperly labeled or contaminated samples
  • Degraded DNA

Understanding Your Results

Results indicate whether pathogenic mutations in the CCDC39 gene are detected, which can confirm or rule out PCD Type 14.
📊

Pathogenic variant detected

Confirms diagnosis of Primary Ciliary Dyskinesia Type 14. Genetic counseling and management recommended.

📊

No pathogenic variant detected

PCD Type 14 is unlikely, but clinical correlation is necessary. Consider other genetic or non-genetic causes.

⚠️ When to Consult a Doctor:

Consult a doctor if you experience symptoms of PCD or for family planning if there is a family history.

Limitations

  • May not detect all genetic variants
  • Requires interpretation by a geneticist
  • Does not rule out other forms of PCD

Risks & Considerations

  • Minimal risk from blood draw
  • Potential psychological impact of genetic results
  • Privacy concerns with genetic data

Interfering Factors

  • Sample contamination
  • Degraded DNA
  • Technical errors in sequencing

Compare With Similar Tests

TestCCDC39 Gene Primary ciliary dyskinesia type 14 NGS Genetic Test
ComparisonCCDC39 Gene Primary ciliary dyskinesia type 14 NGS Genetic Test

Frequently Asked Questions

What is CCDC39 Gene Primary Ciliary Dyskinesia Type 14?
It is a rare genetic disorder caused by mutations in the CCDC39 gene, leading to dysfunction of cilia and symptoms like chronic respiratory infections and fertility issues.
What are the symptoms of PCD Type 14?
Symptoms include chronic cough, recurrent pneumonia, bronchitis, sinusitis, ear infections, nasal congestion, shortness of breath, wheezing, and fertility problems.
How is PCD Type 14 diagnosed?
Diagnosis involves clinical evaluation, high-speed video microscopy, electron microscopy, and genetic testing such as the NGS test for CCDC39 gene.
What is the cost of the CCDC39 Gene NGS Genetic Test?
The test costs 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 online bookings.
How long does it take to get the test results?
Results are typically available within 3 to 4 weeks after sample receipt.
What does a positive test result mean?
A positive result indicates the presence of pathogenic mutations in the CCDC39 gene, confirming PCD Type 14 diagnosis.
Can PCD Type 14 be treated?
While there is no cure, management includes antibiotics for infections, airway clearance techniques, and fertility treatments.
Is genetic testing for PCD covered by insurance?
Coverage varies; it is advisable to check with your insurance provider. DNA Labs India offers competitive pricing.
Who should consider getting this test?
Individuals with symptoms of PCD, a family history of PCD, or those undergoing fertility evaluations.
What is the accuracy of the NGS Genetic Test?
NGS technology provides high accuracy in detecting genetic mutations, but interpretation should be done by a geneticist.
How should I prepare for the test?
No special preparation is needed. A genetic counseling session is recommended before testing.
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 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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