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ST3GAL3 Gene Mental retardation, autosomal recessive type 12 NGS Genetic Test

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ST3GAL3 Gene Mental retardation, autosomal recessive type 12 NGS Genetic Test

Short Name: ST3GAL3 NGS Test

Also known as: ST3GAL3 Gene Sequencing, MRT12 Genetic Test, ST3GAL3 Mutation Analysis

ST3GAL3 Gene Mental retardation, autosomal recessive type 12 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 hours. Free home collection in 300+ cities across India.

NGS Genetic TestAll Ages🏠 Home Collection

🩺 Medically Reviewed By

Overview

The purpose of this test is to identify pathogenic variants in the ST3GAL3 gene that cause autosomal recessive type 12 mental retardation. It is used to confirm a clinical diagnosis, provide prognostic information, guide management, and offer accurate genetic counseling for affected individuals and their families.

Test Code
4253
Price
₹20,000
Sample Type
Blood or Extracted DNA or One drop Blood on FTA Card
Result Time
3 to 4 Weeks hours
Fasting Required
No
Method
Next-Generation Sequencing (NGS)
Step 1

Sample Collection

No special preparation or fasting is required. A pre-test genetic counseling session is recommended to draw a pedigree chart and discuss the implications of results.

Method: Venipuncture or FTA card spot

Step 2

Laboratory Analysis

A blood sample will be collected by a trained phlebotomist. For FTA card samples, a few drops of blood are placed on the card and allowed to dry.

Step 3

Report Delivery

There are no restrictions after sample collection. You can resume normal daily activities immediately.

About This Test

Who Should Get This Test

The purpose of this test is to identify pathogenic variants in the ST3GAL3 gene that cause autosomal recessive type 12 mental retardation. It is used to confirm a clinical diagnosis, provide prognostic information, guide management, and offer accurate genetic counseling for affected individuals and their families.

How to Prepare

  • Blood sample in EDTA tube: 2-3 mL preferred
  • FTA card: one drop of blood spot
  • Extracted DNA: minimum 1 μg in sterile tube
  • Label the sample with patient name, date, and time of collection

Doctor's Notes

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

"Genetic testing is crucial for accurate diagnosis and management of hereditary intellectual disabilities. This NGS test helps identify the underlying genetic cause, enabling informed family planning and personalized care."

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 protocol
ContainerEDTA tube or FTA Card
Collection MethodVenipuncture or FTA card spot

Sample Stability

Whole blood: 24 hours at room temperature (15-25°C)
Whole blood: 7 days at 2-8°C
Extracted DNA: stable for 6 months at -20°C
FTA card spot: stable for several months at room temperature
Sample Rejection Criteria:
  • Hemolyzed or clotted blood sample
  • Incorrectly labeled sample
  • Sample not transported within stability timeframe

Understanding Your Results

Interpretation of this NGS genetic test is provided by qualified clinical geneticists. The report identifies whether any pathogenic or likely pathogenic variants are present in the ST3GAL3 gene, confirms the diagnosis of MRT12, and offers guidance for medical management and family counseling.
📊

No pathogenic variant detected

Negative result. ST3GAL3-associated MRT12 is unlikely; consider other genetic causes.

📊

Pathogenic variant detected (homozygous or compound heterozygous)

Confirms the diagnosis of autosomal recessive type 12 mental retardation.

📊

Variant of uncertain significance (VUS)

Cannot confirm diagnosis. Additional familial testing or functional studies may be recommended.

⚠️ When to Consult a Doctor:

Consult a neurologist or clinical geneticist if you or your child experience unexplained intellectual disability, developmental delay, seizures, speech delay, or have a family history of autosomal recessive mental retardation.

Limitations

  • NGS may not detect large deletions/duplications or trinucleotide repeat expansions
  • A negative result does not exclude a genetic cause; further testing may be required
  • Variants of uncertain significance may need familial segregation analysis

Risks & Considerations

  • No significant physical risks are associated with blood collection. Slight pain or bruising may occur at the needle site.

Interfering Factors

  • Rare benign variants may be reported as variants of uncertain significance
  • Mutations in other genes can mimic MRT12 symptoms

Frequently Asked Questions

What is the cost of the ST3GAL3 gene NGS genetic test?
The cost of the ST3GAL3 Gene Mental Retardation Autosomal Recessive Type 12 NGS Genetic Test at DNA Labs India is INR 20,000. The price includes the NGS analysis of the ST3GAL3 gene and other genes associated with intellectual disability.
What sample is required for this test?
The sample can be blood, extracted DNA, or one drop of blood on an FTA card. The preferred sample type is told at the time of booking.
Is home sample collection available?
Yes, DNA Labs India offers free home sample collection for online bookings of this test across cities like Mumbai, Delhi, Bangalore, Hyderabad, Pune, Chennai, Kolkata, and many more.
How long will the reports take?
The reports are typically delivered within 3 to 4 weeks from the date the sample is received at the laboratory.
What is Mental Retardation, Autosomal Recessive Type 12 (MRT12)?
MRT12 is a rare genetic disorder caused by mutations in the ST3GAL3 gene. It is characterized by intellectual disability, delayed speech and language development, behavioral problems, seizures, and abnormal muscle tone.
Is this test diagnostic for MRT12?
Yes, NGS genetic testing is highly accurate and is the standard method to confirm the diagnosis of MRT12 by identifying pathogenic variants in the ST3GAL3 gene.
Is fasting required before the test?
No, fasting is not required for this genetic test. You can eat and drink normally before sample collection.
Who should consider this test?
Individuals with unexplained intellectual disability, developmental delay, speech delay, behavioral problems, seizures, or a family history of autosomal recessive intellectual disability should consider this test.
Why choose DNA Labs India for this genetic test?
DNA Labs India is a leading provider of genetic testing in India. We use advanced NGS technology, have experienced geneticists, offer transparent reporting with raw data files, and provide free home sample collection across the country.
Will I get the raw data files along with the report?
Yes, DNA Labs India is the only lab that provides RAW DATA, FASTQ, and VCF files along with the conclusive clinical test report. This ensures transparency and allows further analysis if needed.
Is genetic counseling included in this test?
A pre-test genetic counseling session is recommended to draw a pedigree chart reflecting family members affected with the condition. The test process includes this counseling to help you make an informed decision.
Is this test covered by insurance?
Insurance coverage may vary depending on your policy. We recommend checking with your insurance provider to determine if genetic testing is reimbursed.
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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