Skip to main content
DNA Labs India

CEP135 Gene Microcephaly, autosomal recessive type 8 NGS Genetic Test

DNA Labs India | ISO 9001:2015 Certified

CEP135 Gene Microcephaly, autosomal recessive type 8 NGS Genetic Test

Short Name: CEP135 Microcephaly NGS Test

Also known as: CEP135 Gene Test, Microcephaly Type 8 Genetic Test, Autosomal Recessive Microcephaly 8 Test

CEP135 Gene Microcephaly, autosomal recessive 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.

NGS Genetic TestPediatrics🏠 Home Collection

✍️ Written By

🩺 Medically Reviewed By

Dr SHAILAJA RAGHUNATH MURDESHWAR

Dr SHAILAJA RAGHUNATH MURDESHWAR

Consultant Physician · Reg: 8052

Last reviewed: September 7, 2026

Overview

To identify mutations in the CEP135 gene that cause autosomal recessive type 8 microcephaly, aiding in diagnosis, management, and genetic counseling.

Test Code
2767
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

No special preparation required. Provide clinical history and family pedigree.

Method: Venipuncture or finger prick

Step 2

Laboratory Analysis

Blood sample will be collected via venipuncture or finger prick.

Step 3

Report Delivery

Apply pressure to the puncture site to stop bleeding.

Timeline: 3 to 4 weeks

Patient Instructions

1
Before the Test:Consult with a genetic counselor to discuss the test and implications.
2
During the Test:Sample collection and processing in the laboratory.
3
After the Test:Receive report and consult with a specialist for interpretation.

About This Test

Who Should Get This Test

To identify mutations in the CEP135 gene that cause autosomal recessive type 8 microcephaly, aiding in diagnosis, management, and genetic counseling.

How to Prepare

  • Ensure proper identification of the patient
  • Use sterile equipment
  • Label samples correctly

Doctor's Notes

Reviewed by — MBBS, MD (General Medicine) · Reg. No. 8052

"Genetic testing for CEP135 gene mutations is essential for early diagnosis and management of microcephaly, allowing for timely intervention 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 VolumeAs required
ContainerEDTA tube or FTA card
Collection MethodVenipuncture or finger prick

Sample Stability

Blood samples stable at room temperature for 24 hours
Extracted DNA stable at -20°C for long-term storage
Sample Rejection Criteria:
  • Hemolyzed or clotted samples
  • Insufficient sample volume

Understanding Your Results

Results indicate the presence or absence of pathogenic variants in the CEP135 gene.
📊

Normal

No pathogenic variants detected. Clinical correlation recommended.

📊

Abnormal

Pathogenic variant detected. Consistent with autosomal recessive microcephaly type 8. Genetic counseling advised.

⚠️ When to Consult a Doctor:

If symptoms of microcephaly are present or if there is a family history of the condition.

Limitations

  • ⚠Cannot detect all genetic causes of microcephaly
  • ⚠Results may require confirmation with other tests

Risks & Considerations

  • ●Minimal risk from blood draw, such as bruising or infection

Interfering Factors

  • ●Hemolyzed samples may affect DNA quality

Frequently Asked Questions

What is the CEP135 Gene Microcephaly NGS Genetic Test?
It is a genetic test that uses Next Generation Sequencing to detect mutations in the CEP135 gene, which causes autosomal recessive type 8 microcephaly.
Who should take this test?
Infants or children with symptoms like small head size, delayed development, or a family history of microcephaly.
What are the symptoms of CEP135 gene microcephaly?
Symptoms include small head size, delayed development, intellectual disability, seizures, muscle stiffness, and abnormal eye movements.
How is the test performed?
A blood or DNA sample is collected and analyzed using NGS technology to identify gene mutations.
What is the cost of the test?
The test costs INR 20,000 at DNA Labs India.
Is home sample collection available?
Yes, free home sample collection is available for online bookings across India.
How long does it take to get results?
Results are typically available within 3 to 4 weeks.
What do the results mean?
Results indicate if pathogenic variants in the CEP135 gene are detected, which can confirm diagnosis.
Is genetic counseling recommended?
Yes, genetic counseling is advised before and after testing for proper interpretation and guidance.
Can this test be used for prenatal diagnosis?
It is primarily for postnatal diagnosis; consult a specialist for prenatal options.
What are the limitations of the test?
It may not detect all genetic causes of microcephaly and results might need confirmation.
How accurate is the NGS genetic test?
NGS is highly accurate for detecting known mutations, but accuracy depends on sample quality and analysis.
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

Amino Acids Qualitative Two Dimensional Urine Test

₹1,439

Succinylacetone Urine Test

₹5,000

RXFP2 Gene Cryptorchidism NGS Genetic Test

₹20,000

EFNB1 Gene Craniofrontonasal syndrome NGS Genetic Test

₹20,000

MNX1 Gene Currarino syndrome NGS Genetic Test

₹20,000

FGFR1 Gene Craniosynostosis, FGFR1 related 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.