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DYX1C1 Gene Primary ciliary dyskinesia type 25 NGS Genetic Test

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DYX1C1 Gene Primary ciliary dyskinesia type 25 NGS Genetic Test

Short Name: DYX1C1 PCD Type 25 NGS Test

Also known as: PCD Type 25, DYX1C1-related PCD

DYX1C1 Gene Primary ciliary dyskinesia type 25 NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses NGS Technology 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 diagnose PCD Type 25 by detecting mutations in the DYX1C1 gene using NGS technology.

Test Code
4780
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
NGS Technology
Step 1

Sample Collection

No special preparation required.

Method: Venipuncture or FTA card

Step 2

Laboratory Analysis

Blood sample will be drawn by a trained phlebotomist.

Step 3

Report Delivery

Apply pressure to the puncture site to stop bleeding.

Timeline: 3 to 4 weeks

Patient Instructions

1
Before the Test:No special preparation required.
2
During the Test:The NGS analysis is performed in the lab.
3
After the Test:Results are reviewed by a geneticist.

About This Test

Who Should Get This Test

To diagnose PCD Type 25 by detecting mutations in the DYX1C1 gene using NGS technology.

How to Prepare

  • Ensure proper identification
  • Use sterile equipment
  • Label samples correctly

Doctor's Notes

Reviewed by — MBBS, MD (Pathology) · Reg. No. 21521

"Genetic testing for PCD Type 25 is essential for accurate diagnosis and management. It helps in understanding the genetic basis, guiding treatment, and providing family counseling."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Collection MethodVenipuncture or FTA card

Sample Stability

Blood samples stable at room temperature for 24 hours
FTA cards stable for longer periods
Sample Rejection Criteria:
  • Hemolyzed samples
  • Insufficient sample volume

Understanding Your Results

Results indicate the presence or absence of mutations in the DYX1C1 gene associated with PCD Type 25.
📊

Positive

Pathogenic mutation detected, consistent with PCD Type 25

📊

Negative

No pathogenic mutations detected

📊

Variant of uncertain significance

Further testing may be needed

⚠️ When to Consult a Doctor:

If symptoms persist or if there is a family history of PCD, consult a geneticist or pulmonologist.

Limitations

  • Test may not detect all mutations
  • Requires genetic counseling for interpretation

Risks & Considerations

  • Bruising at puncture site
  • Infection at puncture site

Interfering Factors

  • Sample quality
  • DNA degradation

Compare With Similar Tests

TestDYX1C1 Gene Primary ciliary dyskinesia type 25 NGS Genetic TestHigh-speed video microscopyCiliary function testsCT scans of chest and sinusesSemen analysis
ComparisonDYX1C1 Gene Primary ciliary dyskinesia type 25 NGS Genetic Test

Frequently Asked Questions

What is PCD Type 25?
PCD Type 25 is a rare genetic disorder caused by mutations in the DYX1C1 gene, leading to dysfunction of cilia in respiratory, auditory, and reproductive systems.
What causes PCD Type 25?
It is caused by mutations in the DYX1C1 gene, which is involved in cilia formation and function.
What are the symptoms of PCD Type 25?
Common symptoms include chronic cough, recurrent lung infections, shortness of breath, wheezing, hearing loss, and infertility.
How is PCD Type 25 diagnosed?
Diagnosis involves clinical evaluation, ciliary function tests, and genetic testing such as the DYX1C1 gene NGS test.
What is the DYX1C1 gene?
The DYX1C1 gene provides instructions for making a protein essential for cilia formation and function.
What is NGS genetic testing?
NGS (next-generation sequencing) is a high-throughput technology that analyzes DNA sequences to detect genetic mutations accurately.
How accurate is the DYX1C1 gene test?
The NGS test is highly accurate and can detect even small mutations, but interpretation requires genetic counseling.
What is the cost of the test?
The test costs INR 20,000 at DNA Labs India.
Is home sample collection available?
Yes, free home sample collection is available for online bookings across India.
How long does it take to get results?
Results are typically available in 3 to 4 weeks.
What should I do if I test positive?
Consult a healthcare provider or geneticist for management options, genetic counseling, and family planning advice.
Is genetic counseling necessary?
Yes, genetic counseling is recommended to understand test results, inheritance patterns, and implications for family members.
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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Stored in India: All patient records are stored on servers located in India. No data is transferred outside the country.

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