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TANC2 Gene TANC2 related brain disorders NGS Genetic Test

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TANC2 Gene TANC2 related brain disorders NGS Genetic Test

Short Name: TANC2 NGS Test

Also known as: TANC2 gene sequencing, TANC2-related disorder panel, TANC2 NGS analysis

TANC2 Gene TANC2 related brain disorders 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 Reports are typically available within 3 to 4 weeks after sample receipt.. Free home collection in 300+ cities across India.

NGS Genetic TestPediatric, Adult🏠 Home Collection

🩺 Medically Reviewed By

Overview

The purpose of this test is to detect mutations in the TANC2 gene that are associated with neurodevelopmental disorders such as autism, intellectual disability, and developmental delay. Early diagnosis helps in planning therapeutic interventions, genetic counseling, and family planning decisions.

Test Code
5947
CPT Code
81407
ICD Code
F84.9, F70.9, F80.9, F88
Price
₹20,000
Sample Type
Blood or Extracted DNA or One drop Blood on FTA Card
Result Time
Reports are typically available within 3 to 4 weeks after sample receipt.
Fasting Required
No
Method
Next-Generation Sequencing (NGS)
Step 1

Sample Collection

No fasting required. Inform your doctor about any medications or supplements. A genetic counseling session is recommended before the test.

Method: Venipuncture or Finger prick

Step 2

Laboratory Analysis

Blood sample will be collected by a trained phlebotomist. For FTA card, a simple finger prick is sufficient.

Step 3

Report Delivery

No special precautions. You can resume normal activities immediately.

Timeline: Reports are typically available within 3 to 4 weeks after sample receipt.

Patient Instructions

1
Before the Test:A pre-test genetic counseling session is recommended to discuss the purpose, limitations, and implications of the test.
2
During the Test:The test involves a simple blood draw or FTA card sample. No pain or special preparation required.
3
After the Test:You will receive the report via email/portal within 3-4 weeks. A post-test counseling session is advised to understand the results.

About This Test

Who Should Get This Test

The purpose of this test is to detect mutations in the TANC2 gene that are associated with neurodevelopmental disorders such as autism, intellectual disability, and developmental delay. Early diagnosis helps in planning therapeutic interventions, genetic counseling, and family planning decisions.

How to Prepare

  • Blood sample should be collected in an EDTA tube.
  • If using FTA card, ensure the blood spot is completely dried before packaging.
  • Label the sample with patient name, date of birth, and collection date.
  • Transport the sample to the lab within 24 hours at ambient temperature.

Doctor's Notes

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

"TANC2 mutations are rare but significant causes of neurodevelopmental disorders. Early genetic diagnosis enables tailored management and family counseling."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Sample Volume2-3 ml blood or 1 FTA card spot
ContainerEDTA tube or FTA card
Collection MethodVenipuncture or Finger prick

Sample Stability

Blood in EDTA: 24-48 hours at 2-8°C
Extracted DNA: 1 week at -20°C
FTA card: Stable for months at room temperature
Sample Rejection Criteria:
  • Hemolyzed or clotted blood sample
  • Insufficient sample volume
  • Incorrect labeling
  • Sample received after prolonged transit time (>72 hours)

Understanding Your Results

The test report will indicate whether a pathogenic or likely pathogenic variant is identified in the TANC2 gene. Results should be interpreted by a qualified geneticist in the context of clinical findings.
📊

Positive (Pathogenic variant)

Confirms the diagnosis of TANC2-related disorder. Genetic counseling is recommended for the family.

Action: Discuss management options and family planning.

📊

Negative (No variant)

No disease-causing variant found in TANC2. Other genetic or non-genetic causes should be considered.

Action: Further evaluation by a specialist may be needed.

📊

Variant of Uncertain Significance (VUS)

A variant was found but its clinical significance is unknown. Additional testing or family studies may help.

Action: Consult with a geneticist for further analysis.

⚠️ When to Consult a Doctor:

Consult a doctor if you or your child experience developmental delays, intellectual disability, speech difficulties, or behavioral issues. Early diagnosis can lead to better outcomes.

Limitations

  • This test only analyzes the TANC2 gene; other genetic causes may not be detected.
  • Variant of uncertain significance (VUS) may be reported; further testing may be needed.
  • NGS may not detect large deletions/duplications or deep intronic variants.
  • Test does not assess non-genetic causes of symptoms.

Risks & Considerations

  • Minimal risk of bruising or infection at the blood draw site
  • Psychological impact of genetic results
  • Possibility of finding variants of uncertain significance

Interfering Factors

  • Contaminated or degraded DNA sample
  • Insufficient sample quantity
  • Presence of maternal cell contamination (if blood from cord)
  • Recent blood transfusion (within 2 weeks)

Compare With Similar Tests

TestTANC2 Gene TANC2 related brain disorders NGS Genetic TestWhole Exome Sequencing (WES)Chromosomal Microarray (CMA)
ComparisonTANC2 Gene TANC2 related brain disorders NGS Genetic Test

Frequently Asked Questions

What is the TANC2 gene?
The TANC2 gene provides instructions for making a protein involved in brain development and synaptic function. Mutations can lead to neurodevelopmental disorders.
What conditions are associated with TANC2 mutations?
TANC2 mutations are linked to autism spectrum disorder, intellectual disability, developmental delay, ADHD, and speech/language disorders.
How is the TANC2 NGS test performed?
A blood sample or FTA card sample is collected. DNA is extracted and the TANC2 gene is sequenced using NGS technology.
What is the cost of the TANC2 NGS test at DNA Labs India?
The test costs INR 20,000, which includes home sample collection and the clinical report.
How long does it take to get the results?
Reports are typically available within 3 to 4 weeks after the sample reaches the lab.
Is fasting required before the test?
No, fasting is not required for this genetic test.
Can the test be done on children?
Yes, the test is suitable for children and adults. For children, a blood sample or FTA card can be used.
Will I receive raw data files?
Yes, DNA Labs India provides raw data files (FASTQ, VCF) along with the clinical report for transparency.
What is the sample type for this test?
The sample can be blood, extracted DNA, or one drop of blood on an FTA card.
Is genetic counseling included?
Yes, a genetic counseling session is included to draw a pedigree chart and discuss the implications.
Are there any risks associated with the test?
The test is safe with minimal risks like bruising at the blood draw site. Genetic results may have psychological implications.
Can this test detect all genetic causes of brain disorders?
No, this test only analyzes the TANC2 gene. Other genetic causes may require additional testing.
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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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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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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