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MAPK10 Gene Epileptic encephalopathy, Lennox-Gastaut type NGS Genetic Test

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MAPK10 Gene Epileptic encephalopathy, Lennox-Gastaut type NGS Genetic Test

Short Name: MAPK10 Gene LGS NGS Genetic Test

Also known as: MAPK10 Gene Epileptic Encephalopathy NGS Test, Lennox-Gastaut Syndrome MAPK10 Gene Test, MAPK10 Next Generation Sequencing Test

MAPK10 Gene Epileptic encephalopathy, Lennox-Gastaut type NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses Next-Generation Sequencing (NGS), Targeted Gene Sequencing on Blood or Extracted DNA or One drop Blood on FTA Card samples. Results in Reports are delivered within 3 to 4 weeks after the sample reaches the laboratory.. Free home collection in 300+ cities across India.

NGS Genetic Test🏠 Home Collection

🩺 Medically Reviewed By

Overview

The purpose of this NGS genetic test is to identify disease-causing pathogenic or likely pathogenic variants in the MAPK10 gene that may be responsible for Lennox-Gastaut syndrome. A confirmed molecular diagnosis assists clinicians in clinical management, neurodevelopmental surveillance, and family counselling regarding recurrence risk.

Test Code
4088
Price
₹20,000
Sample Type
Blood or Extracted DNA or One drop Blood on FTA Card
Result Time
Reports are delivered within 3 to 4 weeks after the sample reaches the laboratory.
Fasting Required
No
Method
Next-Generation Sequencing (NGS), Targeted Gene Sequencing
Step 1

Sample Collection

No fasting is required. Genetic counselling is recommended before the test so that the patient and family understand the purpose, benefits, risks, and possible outcomes. The referring neurologist or geneticist will review the clinical history, seizure types, EEG findings, and family pedigree.

Method: Blood draw / FTA card spot / purified DNA submission

Step 2

Laboratory Analysis

A small blood sample is collected by venipuncture, or a drop of blood is placed on an FTA card. In some cases, extracted DNA may be sent directly to the laboratory. The procedure is quick and involves minimal discomfort.

Step 3

Report Delivery

No special aftercare is needed. The sample is transported to the laboratory for NGS analysis. The patient can resume normal activities and diet immediately after collection.

Timeline: Reports are delivered within 3 to 4 weeks after the sample reaches the laboratory.

Patient Instructions

1
Before the Test:No special preparation is required. However, a pre-test genetic counselling session is recommended to draw a family pedigree and discuss test expectations.
2
During the Test:A blood sample or FTA card sample is collected. The sample is then sent to the laboratory where next-generation sequencing is performed on the MAPK10 gene.
3
After the Test:The patient can continue routine activities. The report is generated and delivered within 3 to 4 weeks. Post-test genetic counselling is advised to understand the results and implications.

About This Test

Who Should Get This Test

The purpose of this NGS genetic test is to identify disease-causing pathogenic or likely pathogenic variants in the MAPK10 gene that may be responsible for Lennox-Gastaut syndrome. A confirmed molecular diagnosis assists clinicians in clinical management, neurodevelopmental surveillance, and family counselling regarding recurrence risk.

How to Prepare

  • For blood: collect in an EDTA tube and label with patient details
  • For FTA card: apply one drop of blood, air-dry completely, and pack safely
  • For extracted DNA: provide sample quality/quantity information alongside the DNA
  • All samples must be labelled with patient name, date of birth, and collection date
  • Maintain sample at ambient temperature unless otherwise instructed by the laboratory

Doctor's Notes

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

"In families with a child suspected to have Lennox-Gastaut syndrome, a precise genetic diagnosis helps guide treatment choices and recurrence-risk counselling. The MAPK10 NGS test is a focused option when MAPK10-related disorder is clinically suspected."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Sample VolumeAs per laboratory instruction
ContainerEDTA tube / DNA vial / FTA card
Collection MethodBlood draw / FTA card spot / purified DNA submission

Sample Stability

Whole blood in EDTA: stable for up to 72 hours at room temperature
FTA card: stable at room temperature for several weeks
Extracted DNA: stable for 1 week at 2-8°C; long-term storage at -20°C recommended
Sample Rejection Criteria:
  • Clotted or hemolysed blood sample
  • Insufficient sample quantity or DNA concentration
  • Improperly labelled or unlabeled sample
  • Leaked or contaminated sample
  • Sample received beyond the recommended transport time

Understanding Your Results

The MAPK10 NGS genetic test analyzes the MAPK10 gene for sequence variants associated with epileptic encephalopathy, Lennox-Gastaut type. Interpretation should be performed by a clinical geneticist or neurologist in the context of the patient's clinical presentation, EEG findings, and family history.
📊

A pathogenic or likely pathogenic variant in MAPK10 was identified. This is consistent with a molecular diagnosis of MAPK10-related Lennox-Gastaut syndrome.

Result type: Positive

📊

No pathogenic or likely pathogenic variant in MAPK10 was detected. This does not exclude MAPK10-related disease due to variants in regions not covered, or an alternate genetic cause.

Result type: Negative

📊

A variant was found but its clinical significance is unknown. Additional familial testing and clinical correlation may be required.

Result type: Variant of Uncertain Significance (VUS)

📊

No clinically significant alteration was identified and the variant is unlikely to be disease-causing.

Result type: Benign / Likely Benign

⚠️ When to Consult a Doctor:

If your child or a family member has recurrent seizures, developmental delay, abnormal EEG, or features suggestive of Lennox-Gastaut syndrome, consult a pediatric neurologist or clinical geneticist. Genetic counselling before and after testing is strongly advised.

Limitations

  • This targeted NGS test analyzes only the MAPK10 gene and does not rule out other genetic causes of Lennox-Gastaut syndrome
  • Standard NGS may not detect large structural variants, deep intronic mutations, or repeat expansions
  • Variants of uncertain significance may require additional testing or familial segregation studies
  • Genetic test results must always be interpreted in the context of clinical and EEG findings

Risks & Considerations

  • No significant medical risks are associated with this genetic test
  • Minor pain or bruising may occur at the blood-draw site
  • Rarely, dizziness or fainting may occur during blood collection

Interfering Factors

  • Poor quality or insufficient quantity of DNA
  • Sample contamination or mix-up
  • Variants outside the coding and splice-site regions analysed
  • Large gene deletions or duplications not reliably detected by standard NGS
  • Mosaicism below the detection threshold of the assay

Compare With Similar Tests

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ComparisonMAPK10 Gene Epileptic encephalopathy, Lennox-Gastaut type NGS Genetic Test

Frequently Asked Questions

What is Lennox-Gastaut syndrome?
Lennox-Gastaut syndrome is a rare and severe epileptic encephalopathy that usually begins in children between 3 and 5 years of age. It is characterized by multiple seizure types, cognitive developmental delays, intellectual disability, and abnormal EEG patterns.
What is the role of the MAPK10 gene in epileptic encephalopathy?
The MAPK10 gene provides instructions for making the JNK3 protein, which participates in cell death, inflammation, and stress response. Mutations in MAPK10 can lead to Lennox-Gastaut type epileptic encephalopathy.
What does this NGS genetic test analyze?
This NGS-based test analyzes the MAPK10 gene for pathogenic or likely pathogenic variants associated with epileptic encephalopathy, Lennox-Gastaut type.
What is the cost of the MAPK10 gene Lennox-Gastaut NGS genetic test?
The test price is INR 20,000. DNA Labs India offers free home sample collection for online bookings in many cities across India.
What sample is required for the test?
The test can be performed on a blood sample, extracted DNA, or one drop of blood on an FTA card.
Is fasting required before the test?
No, fasting is not required for this genetic test. Samples can be collected at any time of the day.
Who should take this test?
The test is recommended for individuals with clinical suspicion of Lennox-Gastaut syndrome, unexplained epileptic encephalopathy, multiple seizure types with developmental delay, or a family history of MAPK10-related epilepsy.
How long does it take to get reports?
Reports are generally available in 3 to 4 weeks after the sample reaches the laboratory.
Do I need genetic counselling before this test?
Yes, genetic counselling is recommended before the test to help understand the purpose, limitations, possible results, and recurrence risk. It also helps in drawing a family pedigree.
Can this test detect all causes of Lennox-Gastaut syndrome?
No, this is a targeted single-gene test. It only detects variants in the MAPK10 gene. Lennox-Gastaut syndrome can also be caused by other genes, which may require a broader epilepsy panel.
Will NGS detect large deletions or duplications in the MAPK10 gene?
Standard NGS may not reliably detect large deletions, duplications, or structural variants. If suspected, additional testing methods may be recommended by the geneticist.
What does a negative result mean?
A negative result means no pathogenic or likely pathogenic variant was detected in the MAPK10 gene. It does not completely rule out a genetic cause, because variants may exist in other genes or in regions not covered by this test.
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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