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MT-ATP8 Gene Cardiomyopathy, apical hypertrophic, and neuropathy, MT-ATP8 related NGS Genetic Test

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MT-ATP8 Gene Cardiomyopathy, apical hypertrophic, and neuropathy, MT-ATP8 related NGS Genetic Test

Short Name: MT-ATP8 NGS Test

Also known as: MT-ATP8 Gene Test, Cardiomyopathy Genetic Test, Neuropathy Genetic Test

MT-ATP8 Gene Cardiomyopathy, apical hypertrophic, and neuropathy, MT-ATP8 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 to 4 weeks. Free home collection in 300+ cities across India.

NGS Genetic Test🏠 Home Collection

🩺 Medically Reviewed By

Overview

To detect mutations in the MT-ATP8 gene associated with cardiomyopathy, apical hypertrophic, and neuropathy for accurate diagnosis and management.

Test Code
5198
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. Provide clinical history and undergo genetic counseling.

Method: Blood Draw

Step 2

Laboratory Analysis

Blood sample will be drawn by a trained phlebotomist using sterile equipment.

Step 3

Report Delivery

Apply pressure to the puncture site to stop bleeding and avoid strenuous activity.

Timeline: 3 to 4 weeks

Patient Instructions

1
Before the Test:Genetic counseling to discuss implications, benefits, and limitations of testing.
2
During the Test:Sample collection and analysis using NGS technology.
3
After the Test:Report delivery, follow-up counseling, and discussion of results with healthcare provider.

About This Test

Who Should Get This Test

To detect mutations in the MT-ATP8 gene associated with cardiomyopathy, apical hypertrophic, and neuropathy for accurate diagnosis and management.

How to Prepare

  • Ensure proper patient identification
  • Use sterile collection tubes
  • Label samples correctly
  • Transport samples at appropriate temperature

Doctor's Notes

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

"Early genetic testing for MT-ATP8 mutations can guide treatment and family planning for affected individuals."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Collection MethodBlood Draw

Sample Stability

Blood samples stable for 48 hours at room temperature
Extracted DNA stable for longer periods if stored properly
Sample Rejection Criteria:
  • Hemolyzed samples
  • Insufficient sample volume
  • Improper labeling or contamination

Understanding Your Results

Results indicate the presence or absence of pathogenic mutations in the MT-ATP8 gene.
📊

Pathogenic variant detected

Confirms diagnosis of MT-ATP8 related disorder; clinical management and genetic counseling recommended.

📊

No pathogenic variant detected

Unlikely to have MT-ATP8 related disorder; consider other genetic or non-genetic causes.

⚠️ When to Consult a Doctor:

If symptoms persist, worsen, or if there is a family history of genetic disorders, consult a geneticist or cardiologist.

Limitations

  • Test only detects known mutations in MT-ATP8 gene
  • May not identify all genetic causes of symptoms
  • Results require clinical correlation

Risks & Considerations

  • Minimal risk from blood draw such as bruising or infection
  • Emotional impact of genetic results on patient and family

Interfering Factors

  • Sample degradation
  • Contamination during collection or processing

Compare With Similar Tests

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ComparisonMT-ATP8 Gene Cardiomyopathy, apical hypertrophic, and neuropathy, MT-ATP8 related NGS Genetic Test

Frequently Asked Questions

What is the MT-ATP8 Gene Test?
It is a next-generation sequencing (NGS) genetic test to detect mutations in the MT-ATP8 gene associated with cardiomyopathy, apical hypertrophic, and neuropathy.
What symptoms indicate the need for this test?
Symptoms include heart problems like irregular heartbeat, muscle weakness, nerve damage, vision or hearing issues, and cognitive problems.
How is the test performed?
A blood sample is collected and analyzed using NGS technology to identify mutations in the MT-ATP8 gene.
What is the cost of the test?
The test costs INR 20,000 in India, with home sample collection available.
How long does it take to get results?
Results are typically available within 3 to 4 weeks after sample collection.
Is home sample collection available?
Yes, free home sample collection is offered for online bookings across India.
What does a positive result mean?
A positive result indicates a pathogenic mutation in the MT-ATP8 gene, confirming the disorder and guiding management.
Can this test be used for prenatal diagnosis?
Consult a geneticist for prenatal testing options, as this test may not be standard for prenatal use.
Are there any risks associated with the test?
Risks are minimal, mainly related to blood draw, but genetic results may have emotional implications.
How accurate is the NGS genetic test?
NGS is highly accurate for detecting known mutations, but accuracy depends on sample quality and mutation coverage.
What should I do after receiving the results?
Discuss results with a healthcare provider or genetic counselor for appropriate management and family planning.
Is genetic counseling recommended?
Yes, genetic counseling is recommended before and after testing to understand implications and support decision-making.
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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For Hospitals & Clinics

Reference 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.

LIMS Integration

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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