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Medical information Clinical review pending

Genetic Testing

MTO1 Gene Combined Oxidative Phosphorylation Deficiency Type 10 Genetic Test

This genetic test identifies mutations in the MTO1 gene, which can cause Combined Oxidative Phosphorylation Deficiency Type 10, a metabolic disorder affecting energy production. It uses Next-Generation Sequencing (NGS) technology.

General information only: This page is not a diagnosis or personal medical advice. A qualified clinician should decide whether testing is appropriate and interpret results in context.

Review status: No completed medical review is recorded for this page.

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Counselor guidance included Confidential handling Kenya-wide coordination

At a glance

Plan your test

Sample
Blood sample (usually collected in an EDTA tube). Confirm specific requirements with the laboratory before booking.
Results
Confirm with the laboratory before booking.
Preparation
No special preparation is typically required for this test. However, confirm with the laboratory for any specific instructions.
Test priceKSh 40,000

Payment: M-Pesa and card options can be confirmed during booking.

Insurance & government schemes

Is this test covered for you?

We help you verify whether the MTO1 Gene Combined Oxidative Phosphorylation Deficiency Type 10 Genetic Test test can be claimed against your insurer, employer scheme or a Kenyan government health scheme — before you book. Coverage depends on your plan, clinical indication and your provider's rules; final approval always rests with them.

Talk to a claims advisor

Providers & schemes we can help you check

Government & public schemes

SHIF — Social Health Insurance Fund Linda Mama EduAfya NHIF (legacy cards)

Eligibility and benefits follow the current rules of the Social Health Authority (SHA) and applicable government programmes.

Private insurers & employer schemes

Jubilee Health AAR APA Britam CIC Madison Resolution Pioneer Minet Old Mutual GA Life Heritage + other licensed insurers

Names shown for identification only — listing does not imply partnership or guarantee of coverage.

Have these ready when we check

  • Insurer or scheme name & policy / member number
  • A clinician's request / prescription for the test
  • Pre-authorisation letter, if your plan requires one

Free coverage check

Ask us to verify your cover

Send your details and our claims team confirms what documents you need and whether pre-authorisation applies — usually the same working day.

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Used only to process your coverage check — see our Privacy Policy. Verification support is free and does not guarantee your provider will pay.

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01

Start with fit

Is this the right test for you?

The best test starts with a clear clinical question. These are common reasons a clinician or family may consider this test.

  • ✓Individuals with symptoms of metabolic dysfunction (e.g., fatigue, muscle weakness, neurological issues).
  • ✓Patients with a family history of mitochondrial disorders or oxidative phosphorylation deficiencies.
  • ✓Confirmation of suspected Combined Oxidative Phosphorylation Deficiency Type 10.
  • ✓Genetic counseling for families with affected members.
  • ✓Evaluation of unexplained developmental delays or neurological problems.
02

In plain language

What this test helps you understand

This test helps identify specific genetic mutations in the MTO1 gene associated with Combined Oxidative Phosphorylation Deficiency Type 10. Identifying these mutations can confirm a diagnosis, help understand the underlying cause of metabolic symptoms, and provide information for genetic counseling and family planning.
The MTO1 Gene Combined Oxidative Phosphorylation Deficiency Type 10 NGS Genetic DNA Test is a diagnostic tool used to identify genetic mutations linked to metabolic disorders. This test employs Next-Generation Sequencing (NGS) technology to analyze the MTO1 gene, which plays a key role in mitochondrial function and cellular energy production. Understanding variations in this gene can help diagnose conditions related to oxidative phosphorylation deficiencies. This test is particularly relevant for individuals presenting with symptoms suggestive of metabolic dysfunction or those with a family history of related disorders. Results can inform diagnosis, guide treatment strategies, and aid in genetic counseling.
03

Medical review status

Clinical review pending

A completed medical review is not recorded for this page. No clinician has endorsed the information shown here. Please discuss testing decisions with a qualified healthcare professional.

Meet the DNA Labs Kenya medical team →
04

A simple process

What happens next?

You do not have to navigate the test alone. We help you move from question to next step.

1

Speak with us

We check the test and answer your questions before collection.

2

Give your sample

Choose home collection or a coordinated hub visit in Kenya. We explain whether this test uses a cheek swab or blood draw.

3

Understand your report

A counselor helps you understand the result and the next steps.

05

Choose your collection

Home collection or a lab visit

We will explain the sample, preparation, and next steps before anything is collected.

Home collection

Choose a coordinated visit at home or another convenient location. Our team confirms the appointment and sample requirements in advance.

Lab or hub visit

Prefer to visit a coordinated location? We can guide you to the right hub and explain what to expect when you arrive.

Ask about locations →
PreparationNo special preparation is typically required for this test. However, confirm with the laboratory for any specific instructions.
SampleBlood sample (usually collected in an EDTA tube). Confirm specific requirements with the laboratory before booking.
MethodologyNext-Generation Sequencing (NGS) of the MTO1 gene.
PrivacyYour sample and report are handled confidentially. Ask the team how your information is stored and shared.
This test analyzes the MTO1 gene specifically. It may not detect mutations in other genes that can cause similar symptoms. Results should be interpreted alongside clinical findings. The test may not identify all possible variants within the MTO1 gene.
06

Read your report

What common result terms mean

PositiveA finding was identified. Your clinician or counselor will explain what it means for your care.
NegativeThe specific finding tested for was not identified. It does not rule out every possible cause.
VUSA variant was found, but current evidence is not enough to classify it. Your counselor can explain follow-up.
07

Questions people ask

Frequently asked questions

This is a genetic disorder affecting the mitochondria, the energy-producing parts of cells. It is caused by mutations in the MTO1 gene and can lead to various symptoms depending on the severity.
Individuals experiencing symptoms like unexplained fatigue, muscle weakness, or neurological problems, especially if there is a family history of similar conditions, may be candidates for this test.
A blood sample is typically required for this test. We offer convenient home sample collection services in major areas. Confirm collection details with the laboratory.
Confirm with the laboratory before booking.
Results will indicate whether specific mutations in the MTO1 gene were detected. A healthcare provider or genetic counselor will interpret these results in the context of your health history.
08

Collaboration

Open for partnership with hospitals, clinics, doctors & researchers

Whether you are referring patients, building a research programme or supporting students, we work as an extension of your team — with responsive communication and clear scientific standards.

Hospitals & clinics

Referral pathways, coordinated sample logistics and shared reporting that fits your clinical workflow.

Doctors & specialists

LOINC-coded reports, ACMG-based variant classification and a direct scientific line for complex cases.

Research institutions

Sanger sequencing, NGS panels and custom assays — with project design support, batch pricing and agreed turnaround commitments.

Students & academic projects

Discounted laboratory services for college, master's and PhD research projects — including proposal guidance and cost-effective batch testing.

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09

Trust & transparency

Sources, standards & how this page is maintained

Standards & references

  • ACMG/AMP technical standards for sequence variant interpretation
  • ClinGen curation and gene–disease validity frameworks where applicable
  • LOINC-coded reporting for interoperable results
  • ISO 9001:2015 quality management; ISO 15189 accreditation in progress

Page provenance

  • Last updated: September 27, 2026
  • Medical review: not yet completed
  • Written for patients & clinicians in Kenya; reviewed periodically against current guidance

Medical disclaimer: this page is general information, not a diagnosis or personal medical advice. Testing decisions and result interpretation should be made with a qualified healthcare professional.

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