Medical information Clinical review pending

Genetic Testing

LAMTOR2 Gene Immunodeficiency Due to Defect in MAPBP-Interacting Protein Genetic Test

Genetic test using Next-Generation Sequencing (NGS) to identify defects in the MAPBP-interacting protein (LAMTOR2 gene), aiding in the diagnosis of specific immunodeficiency disorders.

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 with the laboratory before booking.
Results: Confirm with the laboratory before booking.
Preparation: No specific fasting is required. Please provide a detailed clinical history and family history (pedigree chart if possible) to the laboratory before the test. Discuss any medications you are taking with your doctor.

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 LAMTOR2 Gene Immunodeficiency Due to Defect in MAPBP-Interacting Protein 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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Mobile number *

+254

Insurer or scheme

Policy / member number (optional)

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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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.

✓Recurrent or severe infections
✓Unusual skin conditions suggestive of immunodeficiency
✓Family history of immunodeficiency disorders
✓Clinical suspicion of LAMTOR2-related immunodeficiency
✓Evaluation of immune system dysfunction
✓Genetic counseling for affected families

In plain language

What this test helps you understand

This test helps identify genetic mutations in the LAMTOR2 gene associated with immunodeficiency disorders. It aids in confirming a diagnosis, understanding the underlying cause of immune dysfunction, and guiding treatment strategies. Results can also inform family planning and risk assessment for relatives.

The LAMTOR2 Gene Immunodeficiency Test is a genetic diagnostic tool that uses Next-Generation Sequencing (NGS) technology. It is designed to detect mutations in the LAMTOR2 gene, which are associated with certain types of immunodeficiency disorders. This test helps identify defects in the MAPBP-interacting protein, a component crucial for proper immune function. Understanding these genetic changes is important for diagnosing the cause of immunodeficiency and guiding appropriate medical management. This test is particularly relevant for individuals with a clinical history suggesting immune system problems. Results provide valuable information for diagnosis, treatment planning, and understanding potential risks for family members. A genetic counseling session is recommended to help interpret the results and discuss their implications.

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.

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A simple process

What happens next?

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

Speak with us

We check the test and answer your questions before collection.

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.

Understand your report

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

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 specific fasting is required. Please provide a detailed clinical history and family history (pedigree chart if possible) to the laboratory before the test. Discuss any medications you are taking with your doctor.

SampleBlood sample (usually collected in an EDTA tube). Confirm with the laboratory before booking.

MethodologyNext-Generation Sequencing (NGS) of the LAMTOR2 gene.

PrivacyYour sample and report are handled confidentially. Ask the team how your information is stored and shared.

This test detects mutations within the LAMTOR2 gene. It may not detect all possible genetic causes of immunodeficiency. Results need to be interpreted by a qualified healthcare professional, often in conjunction with clinical findings. The test may not identify variants of unknown significance.

Read your report

What common result terms mean

TermPlain-language meaning

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.

Questions people ask

Frequently asked questions

The LAMTOR2 gene provides instructions for making a protein involved in immune system function. Mutations in this gene can lead to immunodeficiency disorders.

Individuals with frequent infections, unusual skin conditions, or a family history of immunodeficiency may be candidates for this test. Your doctor will determine if it's appropriate.

The test requires a blood sample. We also require a detailed clinical and family history before testing.

Results are interpreted by genetic specialists. A genetic counseling session is highly recommended to understand the findings and their implications for your health and family.

Genetic counseling is recommended to discuss the test and results but may be arranged separately. Please inquire for details.

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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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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