Skip to main content
DNA Labs India

CEP164 Gene Nephronophthisis type 15 NGS Genetic Test

DNA Labs India | ISO 9001:2015 Certified

CEP164 Gene Nephronophthisis type 15 NGS Genetic Test

Short Name: NPHP15 NGS Test

Also known as: Nephronophthisis type 15, NPHP15, CEP164 gene test, NPHP15 NGS test

CEP164 Gene Nephronophthisis type 15 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, typically childhood/adolescence onset🏠 Home Collection

✍️ Written By

🩺 Medically Reviewed By

Dr Pasupathy Arumugam

Dr Pasupathy Arumugam

Consultant Pathologist · Reg: 21521

Last reviewed: September 7, 2026

Overview

To diagnose Nephronophthisis type 15 by detecting pathogenic mutations in the CEP164 gene using Next-Generation Sequencing (NGS), aiding in early intervention and family planning.

Test Code
5467
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 Nephronophthisis type 15.

Method: Blood draw or FTA card collection

Step 2

Laboratory Analysis

Your sample is analyzed using Next-Generation Sequencing (NGS) in our laboratory.

Step 3

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

Patient Instructions

1
Before the Test:Genetic counseling and clinical history review are recommended before testing.
2
During the Test:Sample collection via blood draw or FTA card.
3
After the Test:Results are delivered in 3-4 weeks via online portal, email, or WhatsApp.

About This Test

Who Should Get This Test

To diagnose Nephronophthisis type 15 by detecting pathogenic mutations in the CEP164 gene using Next-Generation Sequencing (NGS), aiding in early intervention and family planning.

How to Prepare

  • Collect blood sample via venipuncture or use FTA card for one drop of blood
  • Ensure proper labeling and handling of samples

Doctor's Notes

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

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Collection MethodBlood draw or FTA card collection

Understanding Your Results

Results indicate the presence or absence of mutations in the CEP164 gene. A positive result confirms diagnosis, while a negative result may require further testing if clinical suspicion remains.
📊

Mutation Detected

Confirms diagnosis of Nephronophthisis type 15. Genetic counseling and nephrology consultation recommended.

📊

No Mutation Detected

No pathogenic variants found in CEP164 gene. Consider other genetic or non-genetic causes if symptoms persist.

⚠️ When to Consult a Doctor:

If symptoms of nephronophthisis are present, such as increased thirst, reduced urine output, or high blood pressure, or if there is a family history of the disorder.

Limitations

  • ⚠May not detect all genetic variants due to technical limitations
  • ⚠Results require interpretation by a genetic counselor or specialist

Risks & Considerations

  • ●Minimal physical risks from blood draw
  • ●Potential psychological impact of genetic results

Frequently Asked Questions

What is CEP164 Gene Nephronophthisis Type 15?
It is a rare genetic disorder affecting the kidneys, caused by mutations in the CEP164 gene, leading to cilia dysfunction and kidney damage.
What are the common symptoms of NPHP15?
Symptoms include increased thirst and urination, reduced urine output, high blood pressure, swelling in legs and ankles, fatigue, weakness, pale skin, anemia, and delayed growth.
How is Nephronophthisis type 15 diagnosed?
Diagnosis involves clinical evaluation, family history, imaging tests, blood/urine tests, and genetic testing such as NGS to detect CEP164 gene mutations.
What is the cost of the CEP164 Gene NGS Genetic Test in India?
The cost is approximately INR 20,000, which may vary by laboratory and includes home sample collection.
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 via online portal, email, or WhatsApp.
Is the genetic test covered by insurance?
Some insurance plans may cover genetic testing, but it is advisable to check with your provider. Coverage varies.
What is the accuracy of NGS testing for NPHP15?
NGS is a highly accurate method for detecting gene mutations, including rare variants, but results should be interpreted by a genetic specialist.
Can this test be performed on children?
Yes, the test can be done on individuals of all ages, especially if symptoms appear in childhood or adolescence.
What should I do if the test result is positive?
Consult a nephrologist and genetic counselor for management options, family screening, and support.
Are there any risks associated with genetic testing?
Risks are minimal, such as discomfort from blood draw, but there may be psychological impacts; genetic counseling is recommended.
How can I book the CEP164 Gene NGS Genetic Test?
You can book online through DNA Labs India's website or contact them via phone or WhatsApp for assistance.
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.

Related Tests

Amyloid Protein Identification Test

₹300,000

CLCNKB Gene Bartter syndrome type 3 NGS Genetic Test

₹20,000

SLC12A7 Gene Bartter syndrome NGS Genetic Test

₹20,000

SLC12A5 Gene Bartter syndrome NGS Genetic Test

₹20,000

SLC12A2 Gene Bartter syndrome NGS Genetic Test

₹20,000

KCNJ1 Gene Bartter syndrome type 2 NGS Genetic Test

₹20,000
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

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.

Book Your Test

Enter your details and we'll connect you within 15 minutes.

🧬

Quick Connect

Enter your mobile number and we’ll connect you with the team.

+91

✅ Connecting you now...

🔒 Your number is used to respond to this request.