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MOGS Gene Glycosylation disorder type 2B NGS Genetic Test

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MOGS Gene Glycosylation disorder type 2B NGS Genetic Test

Short Name: MOGS Gene NGS Test

Also known as: Congenital Disorder of Glycosylation Type IIb, CDG Type 2B, MOGS-CDG

MOGS Gene Glycosylation disorder type 2B NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses Next-Generation Sequencing (NGS) on Blood or Extracted DNA or One drop Blood on FTA Card samples. Results in 3 to 4 Weeks. Free home collection in 300+ cities across India.

NGS Genetic TestAll Ages🏠 Home Collection

✍️ Written By

🩺 Medically Reviewed By

Dr SULOCHANA HEMCHANDRA HOLLA

Dr SULOCHANA HEMCHANDRA HOLLA

Consultant Medical Geneticist · Reg: 8532

Last reviewed: September 7, 2026

Overview

The purpose of this test is to detect pathogenic variants in the MOGS gene to diagnose Glycosylation Disorder Type 2B, enabling early management, family counseling, and informed medical decisions.

Test Code
2050
Price
₹20,000
Sample Type
Blood or Extracted DNA or One drop Blood on FTA Card
Result Time
3 to 4 Weeks
Fasting Required
No
Method
Next-Generation Sequencing (NGS)
Step 1

Sample Collection

Clinical history of the patient and a genetic counseling session to draw a pedigree chart of family members affected with Glycosylation Disorder Type 2B.

Method: Venipuncture

Step 2

Laboratory Analysis

Standard blood draw or DNA collection from FTA card.

Step 3

Report Delivery

Sample is processed for NGS analysis in the laboratory.

Timeline: 3 to 4 Weeks

Patient Instructions

1
Before the Test:Genetic counseling session and collection of clinical history.
2
During the Test:NGS analysis of the MOGS gene from the provided sample.
3
After the Test:Report generation and delivery via chosen method.

About This Test

Who Should Get This Test

The purpose of this test is to detect pathogenic variants in the MOGS gene to diagnose Glycosylation Disorder Type 2B, enabling early management, family counseling, and informed medical decisions.

How to Prepare

  • Ensure proper labeling of samples
  • Use sterile collection tubes
  • Transport at ambient room temperature

Doctor's Notes

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

"Early diagnosis is important in managing symptoms and providing supportive care for MOGS Gene Glycosylation Disorder Type 2B."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Sample VolumeVaries
ContainerEDTA tube or FTA card
Collection MethodVenipuncture

Sample Stability

Blood samples stable at room temperature for 24 hours
Extracted DNA stable at -20°C for long-term storage
Sample Rejection Criteria:
  • Hemolyzed samples
  • Insufficient sample volume
  • Contaminated or unlabeled samples

Understanding Your Results

Results indicate the presence or absence of pathogenic variants in the MOGS gene, aiding in diagnosis.
📊

No pathogenic variants detected

Normal result; does not rule out other genetic disorders.

📊

Pathogenic variant detected

Confirmatory for MOGS Gene Glycosylation Disorder Type 2B; clinical correlation recommended.

⚠️ When to Consult a Doctor:

If symptoms of developmental delay, seizures, or other indicators are present, or for family planning in cases with family history.

Limitations

  • ⚠May not detect all genetic variants
  • ⚠Requires genetic counseling for interpretation
  • ⚠Results are indicative and may need confirmatory testing

Risks & Considerations

  • ●Minor bruising or infection at blood draw site
  • ●Psychological impact of results

Interfering Factors

  • ●Sample contamination
  • ●Degraded DNA
  • ●Improper sample storage

Frequently Asked Questions

What is MOGS Gene Glycosylation Disorder Type 2B?
It is a rare genetic disorder affecting the glycosylation process, leading to symptoms like developmental delay and seizures.
What are the common symptoms of this disorder?
Symptoms include developmental delay, intellectual disability, seizures, abnormal facial features, and failure to thrive, usually appearing in infancy.
How is MOGS Gene Glycosylation Disorder Type 2B diagnosed?
Diagnosis is through genetic testing, specifically Next-Generation Sequencing (NGS) to detect mutations in the MOGS gene.
What is the cost of the NGS Genetic Test for this disorder in India?
The cost is INR 20000 at DNA Labs India, with free home sample collection available.
Is home sample collection available for this test?
Yes, DNA Labs India offers free home sample collection across India for online bookings.
How long does it take to get the test results?
Results are typically delivered within 3 to 4 weeks.
Is there a cure for MOGS Gene Glycosylation Disorder Type 2B?
No, there is currently no cure; treatment focuses on managing symptoms through supportive care.
What treatments are available for this disorder?
Treatments include physical therapy, speech therapy, and medications to control seizures and other symptoms.
Who should consider getting tested for this disorder?
Individuals with symptoms like developmental delay or seizures, or those with a family history of glycosylation disorders.
What is NGS technology?
NGS (Next-Generation Sequencing) is a high-throughput method that allows for simultaneous analysis of multiple genes, making it efficient for genetic testing.
Are there any risks associated with this genetic test?
Risks are minimal, typically limited to minor discomfort from blood draw, such as bruising or infection.
How should I prepare for the test?
No special preparation is required, but a genetic counseling session is recommended to discuss clinical history and family pedigree.
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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For Hospitals & Clinics

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We serve as a reference laboratory for hospitals and clinics across India. Send samples from your facility with same-day pickup, priority processing, and results delivered through our online portal. Competitive institutional pricing available.

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