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CUL4B Gene Mental retardation, X-linked type 15 NGS Genetic Test

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CUL4B Gene Mental retardation, X-linked type 15 NGS Genetic Test

Short Name: CUL4B MRX15 NGS Test

Also known as: CUL4B-related intellectual disability, X-linked intellectual disability 15

CUL4B Gene Mental retardation, X-linked 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.

Next-Generation Sequencing (NGS)🏠 Home Collection

🩺 Medically Reviewed By

Overview

The purpose of the CUL4B Gene Mental Retardation, X-linked Type 15 NGS Genetic Test is to diagnose genetic mutations in the CUL4B gene that cause X-linked intellectual disability. This test helps confirm clinical suspicions, differentiates from other genetic disorders, provides information for prognosis and management, and supports genetic counseling for affected individuals and their families.

Test Code
1695
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

A genetic counseling session is recommended to discuss the test, draw a pedigree chart of family history, and obtain informed consent. Clinical history of the patient should be reviewed. No fasting is required, and samples should be stored at ambient room temperature.

Method: Venipuncture

Step 2

Laboratory Analysis

Blood sample is collected via venipuncture from a vein in the arm. For FTA card, a finger-prick blood drop is used. The procedure is quick and minimally invasive.

Step 3

Report Delivery

The blood sample or FTA card is labeled, stored properly, and transported to the laboratory under appropriate conditions. Post-collection care includes standard bandaging and observation for any adverse effects.

Timeline: 3 to 4 Weeks

Patient Instructions

1
Before the Test:Genetic counseling to discuss test purpose, implications, and family history. No special preparation required.
2
During the Test:Blood sample collection via venipuncture or FTA card. Procedure takes about 10-15 minutes.
3
After the Test:Apply pressure to the puncture site. Resume normal activities. Results available in 3-4 weeks.

About This Test

Who Should Get This Test

The purpose of the CUL4B Gene Mental Retardation, X-linked Type 15 NGS Genetic Test is to diagnose genetic mutations in the CUL4B gene that cause X-linked intellectual disability. This test helps confirm clinical suspicions, differentiates from other genetic disorders, provides information for prognosis and management, and supports genetic counseling for affected individuals and their families.

How to Prepare

  • Use sterile blood collection tubes or FTA cards
  • Label samples accurately with patient details
  • Store blood samples at ambient temperature if extracting DNA later
  • Avoid hemolysis during collection

Doctor's Notes

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

"This test is crucial for diagnosing CUL4B gene mutations causing X-linked intellectual disability, aiding in accurate diagnosis, 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
Collection MethodVenipuncture

Sample Stability

Sample Rejection Criteria:
  • Hemolyzed samples
  • Insufficient sample volume
  • Contaminated samples
  • Incorrectly labeled samples
  • Samples not collected per instructions

Understanding Your Results

Interpretation of the CUL4B Gene NGS Genetic Test results should be performed by a qualified geneticist or healthcare professional. Results indicate the presence or absence of pathogenic variants in the CUL4B gene.
📊

Positive for pathogenic variant

Confirms diagnosis of X-linked mental retardation type 15 due to CUL4B mutation. Genetic counseling and further clinical management recommended.

📊

Negative for pathogenic variant

No detectable mutations in the CUL4B gene. However, clinical symptoms may still be due to other genetic or non-genetic causes.

📊

Variant of uncertain significance (VUS)

A genetic variant was detected but its clinical significance is unknown. Further testing or family studies may be needed.

📊

Inconclusive

Test could not provide a definitive result due to technical issues. Repeat testing or alternative methods may be considered.

⚠️ When to Consult a Doctor:

Consult a geneticist or neurologist immediately after receiving positive or uncertain results. Also, consult if symptoms persist despite negative results, or for guidance on treatment and family planning.

Limitations

  • May not detect all types of mutations (e.g., large deletions/duplications if not covered by NGS panel)
  • Results require interpretation by a genetic specialist
  • Not all genetic variants have known clinical significance

Risks & Considerations

  • Minor pain or bruising at blood draw site
  • Minimal risk of infection
  • Fainting or dizziness in rare cases

Interfering Factors

  • Hemolyzed or degraded blood samples
  • Contamination during sample collection
  • Insufficient sample volume
  • Incorrect sample storage conditions

Compare With Similar Tests

TestCUL4B Gene Mental retardation, X-linked type 15 NGS Genetic TestFragile X Syndrome Genetic TestRett Syndrome Genetic TestGeneral Intellectual Disability PanelChromosomal Microarray Analysis
ComparisonCUL4B Gene Mental retardation, X-linked type 15 NGS Genetic Test

Frequently Asked Questions

What is the CUL4B Gene Mental Retardation NGS Genetic Test?
It is a genetic test using Next-Generation Sequencing to detect mutations in the CUL4B gene, which is linked to X-linked intellectual disability type 15.
What are the symptoms of CUL4B gene mutation?
Symptoms include intellectual disability, developmental delay, speech delay, behavioral problems, autism, seizures, microcephaly, and facial dysmorphism.
How is the test performed?
The test involves analyzing a blood sample or DNA extract using NGS technology to identify mutations in the CUL4B gene.
What is the cost of this test in India?
The cost is INR 20,000 at DNA Labs India, with free home sample collection available.
Is home sample collection available?
Yes, DNA Labs India offers free home sample collection across many Indian cities for this test.
How long does it take to get results?
Results are typically available within 3 to 4 weeks after sample collection.
Is this test covered by insurance?
Generally, this test is not covered by insurance in India, and payment is usually out-of-pocket.
Who should consider getting this test?
Individuals with symptoms of intellectual disability, especially males with a family history of X-linked conditions, should consider this test.
What is X-linked inheritance?
X-linked inheritance means the gene is located on the X chromosome, with mutations often affecting males more severely due to having only one X chromosome.
What if the test result is positive?
A positive result confirms a CUL4B mutation; consult a geneticist for management, counseling, and family planning advice.
How accurate is NGS for this test?
NGS is highly accurate for detecting single-gene mutations, but all genetic tests have limitations; interpret results with expert guidance.
What should I do after receiving results?
Discuss results with a genetic counselor or healthcare provider to understand implications, management options, and potential family risks.
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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