TMEM127 Gene Pheochromocytoma type 8 NGS Genetic Test
TMEM127 Gene Pheochromocytoma type 8 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.
🩺 Medically Reviewed By
Dr Pasupathy Arumugam
Consultant Pathologist · Reg: 21521
Last reviewed: September 7, 2026
Overview
The purpose of the TMEM127 Gene Pheochromocytoma type 8 NGS Genetic Test is to identify mutations in the TMEM127 gene that cause Pheochromocytoma type 8, an autosomal dominant condition. This test helps in confirming diagnosis, assessing risk for affected individuals and family members, guiding treatment decisions, and facilitating genetic counseling. It is recommended for patients with symptoms of pheochromocytoma, a family history of the condition, or as part of a comprehensive evaluation for adrenal tumors.
- Test Code
- 2927
- 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)
Sample Collection
A certified phlebotomist visits your home or you visit our nearest center. The process takes under 5 minutes.
Laboratory Analysis
Your sample is analyzed using Next Generation Sequencing (NGS) in our laboratory.
Report Delivery
A certified pathologist reviews and signs your report. You receive it as a secure PDF via email and WhatsApp.
Timeline: 3 to 4 Weeks
About This Test
Who Should Get This Test
The purpose of the TMEM127 Gene Pheochromocytoma type 8 NGS Genetic Test is to identify mutations in the TMEM127 gene that cause Pheochromocytoma type 8, an autosomal dominant condition. This test helps in confirming diagnosis, assessing risk for affected individuals and family members, guiding treatment decisions, and facilitating genetic counseling. It is recommended for patients with symptoms of pheochromocytoma, a family history of the condition, or as part of a comprehensive evaluation for adrenal tumors.
Doctor's Notes
Reviewed by Dr Pasupathy Arumugam — MBBS, MD (Pathology) · Reg. No. 21521
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Understanding Your Results
Pathogenic variant detected
Confirms a diagnosis of Pheochromocytoma type 8 and indicates an increased risk for tumor development. Genetic counseling and regular monitoring are recommended.
No pathogenic variant detected
No evidence of TMEM127 gene mutations associated with Pheochromocytoma type 8. However, clinical correlation is advised as other genetic or non-genetic factors may be involved.
Variant of uncertain significance (VUS)
A genetic variant was found, but its clinical significance is unknown. Further testing and family studies may be required for clarification.
Consult a doctor if you experience symptoms such as persistent high blood pressure, headaches, sweating, or palpitations, especially with a family history of pheochromocytoma or related tumors. Early consultation is crucial for timely diagnosis and management.
Frequently Asked Questions
What is the TMEM127 gene?
What is Pheochromocytoma type 8?
What are the common symptoms of Pheochromocytoma type 8?
How is Pheochromocytoma type 8 diagnosed?
What is the cost of the TMEM127 gene test in India?
Is the test covered by insurance?
How long does it take to get the test results?
What sample is required for the test?
Is home sample collection available?
What does a positive test result mean?
What should I do if I have a family history of pheochromocytoma?
How accurate is the NGS genetic test?
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