MT-TQ Gene Myopathy, MT-TQ related NGS Genetic Test
Short Name: MT-TQ Gene Myopathy NGS Test
Also known as: Mitochondrial Myopathy MT-TQ, MT-TQ Related Myopathy
MT-TQ Gene Myopathy, MT-TQ related 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 3-4 weeks. Free home collection in 300+ cities across India.
🩺 Medically Reviewed By
Dr Pasupathy Arumugam
Consultant Pathologist · Reg: 21521
Last reviewed: September 3, 2026
Overview
To diagnose MT-TQ gene myopathy by identifying mutations in the MT-TQ gene using next-generation sequencing technology.
- Test Code
- 5278
- Price
- ₹20,000
- Sample Type
- Blood or Extracted DNA or One drop Blood on FTA Card
- Result Time
- 3-4 weeks
- Fasting Required
- No
- Method
- NGS Technology
Sample Collection
Genetic counseling session and clinical history review.
Method: Venipuncture
Laboratory Analysis
Blood sample collection via venipuncture.
Report Delivery
Sample sent to laboratory for NGS analysis.
Timeline: 3-4 weeks
Patient Instructions
About This Test
Who Should Get This Test
To diagnose MT-TQ gene myopathy by identifying mutations in the MT-TQ gene using next-generation sequencing technology.
How to Prepare
- Use EDTA tube for blood
- Store at 2-8°C
- Ship within 24 hours
Doctor's Notes
Reviewed by Dr Pasupathy Arumugam — MBBS, MD (Pathology) · Reg. No. 21521
"This NGS genetic test is essential for diagnosing MT-TQ gene myopathy, helping to tailor treatment plans and provide genetic counseling for affected families."
Last medically reviewed: September 3, 2026
Test Parameters & Specifications
- Hemolyzed samples
- Insufficient volume
- Improperly labeled samples
Understanding Your Results
Positive
Pathogenic mutation detected, confirming MT-TQ gene myopathy.
Negative
No pathogenic mutation detected, but clinical correlation is needed.
Variant of uncertain significance
Further testing and family studies recommended.
If you experience symptoms such as muscle weakness, fatigue, or have a family history of mitochondrial disorders, consult a healthcare provider for evaluation.
Limitations
- ⚠May not detect all types of mutations
- ⚠Cannot predict disease severity
- ⚠Requires genetic counseling for interpretation
Risks & Considerations
- ●Minor bruising at blood draw site
- ●Infection risk (minimal)
Interfering Factors
- ●Sample contamination
- ●Degraded DNA
- ●Hemolyzed blood samples
Frequently Asked Questions
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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
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✓ 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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