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DNA Labs India

MLC1 Gene Mutation Analysis (Agrawal Mutation) Test

DNA Labs India | ISO 9001:2015 Certified

MLC1 Gene Mutation Analysis (Agrawal Mutation) Test

Also known as: MLC1 gene test, Agrawal mutation test, MLC genetic test

MLC1 Gene Mutation Analysis (Agrawal Mutation) Test test available at DNA Labs India for ₹9,000. Uses Sanger Sequencing on Peripheral blood/Amniotic Fluid/Chorionic Villi/Cord blood samples. Results in 7-8 days. Free home collection in 300+ cities across India.

Genetic Test🏠 Home Collection

🩺 Medically Reviewed By

Overview

The purpose of MLC1 Gene Mutation Analysis is to diagnose mutations in the MLC1 gene, including the Agrawal mutation, to confirm megalencephalic leukoencephalopathy with subcortical cysts (MLC). This helps in accurate diagnosis, management, and genetic counseling for individuals with symptoms or family history of the disorder.

Test Code
3091
Price
₹9,000
Sample Type
Peripheral blood/Amniotic Fluid/Chorionic Villi/Cord blood
Result Time
7-8 days
Fasting Required
No
Method
Sanger Sequencing
Step 1

Sample Collection

MLC1 Gene Mutation Analysis (Agrawal Mutation) can be done with a Doctor’s prescription. Prescription is not applicable for surgery and pregnancy cases or people planning to travel abroad.

Step 2

Laboratory Analysis

Your sample is analyzed using Sanger Sequencing in our laboratory.

Step 3

Report Delivery

A certified pathologist reviews and signs your report. You receive it as a secure PDF via email and WhatsApp.

Timeline: 7-8 days

Patient Instructions

1
Before the Test:Obtain a doctor's prescription unless exempt for surgery, pregnancy, or travel abroad.
2
During the Test:Sample collection via blood draw or other specified methods.
3
After the Test:Results are delivered online within 7-8 days. Follow up with a healthcare provider for interpretation.

About This Test

Who Should Get This Test

The purpose of MLC1 Gene Mutation Analysis is to diagnose mutations in the MLC1 gene, including the Agrawal mutation, to confirm megalencephalic leukoencephalopathy with subcortical cysts (MLC). This helps in accurate diagnosis, management, and genetic counseling for individuals with symptoms or family history of the disorder.

How to Prepare

  • Use sterile container or EDTA Vacutainer
  • Ensure proper labeling
  • Transport with cool pack if needed

Doctor's Notes

Reviewed by — MBBS, MD (Pathology) · Reg. No. 21521

"Genetic testing for MLC1 mutations is crucial for early diagnosis and management of megalencephalic leukoencephalopathy, aiding in genetic counseling and family planning."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypePeripheral blood/Amniotic Fluid/Chorionic Villi/Cord blood
ContainerSterile container/Sterile Normal Saline Container/EDTA Vacutainer (2ml)

Understanding Your Results

Results indicate the presence or absence of pathogenic variants in the MLC1 gene. A positive result confirms a genetic diagnosis of MLC, while a negative result may require further clinical evaluation.
📊

Positive

Pathogenic variant detected, consistent with MLC diagnosis. Consult a geneticist for management.

📊

Negative

No pathogenic variant detected. Symptoms may be due to other causes; consider additional testing.

⚠️ When to Consult a Doctor:

Consult a healthcare provider if you experience symptoms of MLC such as delayed development, seizures, or visual problems, or if you have a family history of the disorder.

Risks & Considerations

  • Minimal physical risks from blood draw
  • Potential psychological impact of genetic results
  • Privacy concerns with genetic data

Frequently Asked Questions

What is MLC1 Gene Mutation Analysis?
It is a genetic test to detect mutations in the MLC1 gene, associated with megalencephalic leukoencephalopathy with subcortical cysts (MLC).
What is the Agrawal mutation?
The Agrawal mutation is a specific pathogenic variant in the MLC1 gene that can cause MLC.
Who should get this test?
Individuals with symptoms of MLC such as delayed development, seizures, or visual problems, or those with a family history of the disorder.
How is the test performed?
The test uses Sanger sequencing on a blood or other tissue sample, collected via home or lab visit.
What is the cost of the test?
The cost at DNA Labs India is INR 9000, with home sample collection available.
Is home sample collection available?
Yes, free home sample collection is offered for online bookings across many cities in India.
How long does it take to get results?
Results are typically available within 7-8 days after sample collection.
Do I need a doctor's prescription?
Yes, a doctor's prescription is required, except for surgery, pregnancy, or travel abroad cases.
What are the symptoms of MLC?
Symptoms include delayed development, difficulty walking, speech difficulties, seizures, abnormal muscle tone, and visual problems.
Can this test be done during pregnancy?
Yes, but a doctor's prescription is not applicable for pregnancy cases; consult your healthcare provider.
Is the test covered by insurance?
Coverage depends on your insurance plan; check with your provider. It is not typically covered under government schemes like PMJAY.
What should I do if the test is positive?
Consult a geneticist or neurologist for further management, genetic counseling, and family planning advice.
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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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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