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Medical information Clinical review pending

Genetic Testing

TMLHE Gene Autism Susceptibility X-Linked Type 6 Genetic Test

The TMLHE Gene Autism Susceptibility X-Linked Type 6 NGS Genetic DNA Test identifies mutations in the TMLHE gene associated with autism spectrum disorders. This test uses Next-Generation Sequencing (NGS) technology to provide insights into genetic predispositions, aiding in early diagnosis and management, particularly for families with a history of autism.

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 (EDTA tube), extracted DNA, or one drop of blood on an FTA card.
Results
Approximately 3 to 4 weeks. Confirm with the laboratory before booking.
Preparation
A clinical history assessment and genetic counseling session, including a pedigree chart of affected family members, are recommended before the test.
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 TMLHE Gene Autism Susceptibility X-Linked Type 6 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.

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 suggestive of autism spectrum disorder.
  • ✓Families with a known history of autism spectrum disorder.
  • ✓Individuals undergoing genetic counseling for developmental delays.
  • ✓Parents seeking to understand genetic risk factors for autism in their child.
02

In plain language

What this test helps you understand

Identifies mutations in the TMLHE gene associated with autism spectrum disorders, potentially aiding in diagnosis, understanding genetic risk, and guiding management strategies.
The TMLHE Gene Autism Susceptibility X-Linked Type 6 NGS Genetic DNA Test is a specialized genetic test designed to identify mutations in the TMLHE gene that may be associated with autism spectrum disorders. This test plays a vital role in understanding the genetic factors contributing to autism, especially for families where autism has been diagnosed. By utilizing Next-Generation Sequencing (NGS) technology, this test offers accurate and comprehensive information about genetic predispositions, which can help guide timely interventions and personalized care plans.

This genetic test specifically analyzes variations within the TMLHE gene, which research has linked to autism susceptibility. By examining an individual's genetic material, healthcare providers can determine if they carry mutations that might increase the risk of developing autism spectrum disorders.

Understanding Your Results

Results from the TMLHE Gene test will be presented in a detailed report outlining any identified mutations. It is crucial to discuss these results with a qualified healthcare professional or genetic counselor. They can help interpret the findings in the context of your personal and family history and guide you on potential next steps, including appropriate therapies or interventions.

Convenient Locations and Booking

We offer testing services across Kenya, including major cities like Nairobi, Mombasa, and Kisumu. For added convenience, we also provide home sample collection services. To book the TMLHE Gene Autism Susceptibility X-Linked Type 6 NGS Genetic DNA Test, please contact us at +254711564616.
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 →
PreparationA clinical history assessment and genetic counseling session, including a pedigree chart of affected family members, are recommended before the test.
SampleBlood sample (EDTA tube), extracted DNA, or one drop of blood on an FTA card.
MethodologyNext-Generation Sequencing (NGS)
PrivacyYour sample and report are handled confidentially. Ask the team how your information is stored and shared.
This test specifically analyzes the TMLHE gene. Autism spectrum disorders can be complex and may be associated with other genes or environmental factors not assessed by this test. A negative result does not rule out autism spectrum disorder. Confirm with the laboratory before booking.
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

The TMLHE gene provides instructions for making a protein involved in cellular processes. Variations in this gene have been linked to an increased risk of developing autism spectrum disorders.
Individuals showing signs of autism or developmental delays, and families with a history of autism spectrum disorders may benefit from this test after consultation with a healthcare provider.
Results are provided in a report detailing any identified mutations. It is essential to discuss these findings with a healthcare professional or genetic counselor for accurate interpretation and guidance.
The test requires a blood sample, extracted DNA, or a single drop of blood collected on a special FTA card.
The turnaround time is typically 3 to 4 weeks from sample receipt. Confirm with the laboratory before booking.
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.

Explore partnerships
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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