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PRKCG Gene Spinocerebellar ataxia type 14, autosomal dominant NGS Genetic Test

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PRKCG Gene Spinocerebellar ataxia type 14, autosomal dominant NGS Genetic Test

Short Name: PRKCG Gene SCA14 NGS Test

Also known as: Spinocerebellar ataxia type 14, SCA14

PRKCG Gene Spinocerebellar ataxia type 14, autosomal dominant NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses NGS Technology on Blood or Extracted DNA or One drop Blood on FTA Card samples. Results in Results are typically available within 3 to 4 weeks after sample receipt.. Free home collection in 300+ cities across India.

NGS Genetic TestAdults🏠 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 the PRKCG Gene Spinocerebellar ataxia type 14 NGS Genetic Test is to diagnose SCA14 by detecting pathogenic mutations in the PRKCG gene, aiding in clinical management and genetic counseling for patients and families.

Test Code
1832
Price
₹20,000
Sample Type
Blood or Extracted DNA or One drop Blood on FTA Card
Result Time
Results are typically available within 3 to 4 weeks after sample receipt.
Fasting Required
No
Method
NGS Technology
Step 1

Sample Collection

Genetic counseling session and clinical history evaluation are required.

Method: Venipuncture or FTA Card Collection

Step 2

Laboratory Analysis

Blood sample collection via venipuncture or FTA card method.

Step 3

Report Delivery

Sample is processed and analyzed using NGS technology at the laboratory.

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

Patient Instructions

1
Before the Test:Genetic counseling and comprehensive clinical evaluation.
2
During the Test:Blood sample collection and processing for NGS analysis.
3
After the Test:Analysis, interpretation, and reporting with genetic counseling.

About This Test

Who Should Get This Test

The purpose of the PRKCG Gene Spinocerebellar ataxia type 14 NGS Genetic Test is to diagnose SCA14 by detecting pathogenic mutations in the PRKCG gene, aiding in clinical management and genetic counseling for patients and families.

How to Prepare

  • A Genetic Counselling session to draw a pedigree chart of family members affected with SCA14

Doctor's Notes

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

"Early genetic testing for SCA14 can aid in timely management and family planning."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Collection MethodVenipuncture or FTA Card Collection

Understanding Your Results

Results indicate the presence or absence of mutations in the PRKCG gene associated with SCA14.
📊

Confirms diagnosis of Spinocerebellar ataxia type 14; clinical management and family screening advised.

📊

No mutation detected; clinical correlation recommended if symptoms persist.

⚠️ When to Consult a Doctor:

If you experience symptoms of ataxia, such as coordination problems or tremors, or if there is a family history of SCA14.

Limitations

  • ⚠May not detect all genetic variants; clinical correlation recommended
  • ⚠Requires genetic counseling for interpretation

Risks & Considerations

  • ●Standard blood draw risks (e.g., bruising, infection)
  • ●Potential psychological impact of genetic diagnosis

Interfering Factors

  • ●Poor DNA quality
  • ●Sample contamination

Compare With Similar Tests

TestPRKCG Gene Spinocerebellar ataxia type 14, autosomal dominant NGS Genetic TestSCA1 Genetic TestSCA2 Genetic Test
ComparisonPRKCG Gene Spinocerebellar ataxia type 14, autosomal dominant NGS Genetic TestTests for mutations in the ATXN1 gene causing SCA1, a different type of spinocerebellar ataxia.Targets ATXN2 gene mutations for SCA2 diagnosis.

Frequently Asked Questions

What is Spinocerebellar ataxia type 14 (SCA14)?
SCA14 is a rare autosomal dominant genetic disorder caused by mutations in the PRKCG gene, leading to progressive coordination and balance issues.
What causes SCA14?
SCA14 is caused by mutations in the PRKCG gene, which is involved in normal cerebellar neuron function.
What are the common symptoms of SCA14?
Symptoms include difficulty with coordination, tremors, speech and swallowing problems, eye movement abnormalities, and mood changes like depression or anxiety.
How is SCA14 diagnosed?
Diagnosis involves clinical evaluation, genetic testing (like the PRKCG Gene NGS Test), and imaging studies such as MRI to rule out other conditions.
What is the PRKCG Gene NGS Genetic Test?
It is a Next-Generation Sequencing test that detects mutations in the PRKCG gene to confirm SCA14 diagnosis.
What does the test involve?
The test requires a blood or DNA sample, which is analyzed using NGS technology. Genetic counseling is included before and after testing.
How much does the test cost in India?
The cost is INR 20,000 at DNA Labs India, with free home sample collection available across major cities.
Is home sample collection available?
Yes, DNA Labs India offers free home sample collection for this test in many Indian cities.
How long does it take to get results?
Results are typically available within 3 to 4 weeks after sample collection.
What should I do if I have a family history of SCA14?
Consider genetic testing and counseling to understand your risk and implications for family members.
Can SCA14 be cured?
There is no cure for SCA14, but early diagnosis can help manage symptoms and improve quality of life through supportive therapies.
Where can I get this test done?
DNA Labs India provides this test nationwide; you can book online for home sample collection or visit a walk-in center.
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

Reference Laboratory Services

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.

LIMS Integration

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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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