LCK Gene Immunodeficiency type 22 NGS Genetic Test
Short Name: LCK Immunodeficiency Type 22 Test
Also known as: LCK-related immunodeficiency, Immunodeficiency Type 22
LCK Gene Immunodeficiency type 22 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 3 to 4 Weeks. Free home collection in 300+ cities across India.
🩺 Medically Reviewed By
Dr SULOCHANA HEMCHANDRA HOLLA
Consultant Medical Geneticist · Reg: 8532
Last reviewed: September 7, 2026
Overview
To diagnose LCK Gene Immunodeficiency Type 22 by identifying mutations in the LCK gene using NGS technology, aiding in clinical management and genetic counseling.
- Test Code
- 5010
- 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
- NGS Technology
Sample Collection
Provide clinical history and undergo genetic counseling to draw a pedigree chart of affected family members.
Method: Venipuncture or blood drop
Laboratory Analysis
Blood sample collected via venipuncture or one drop on FTA card by a trained professional.
Report Delivery
Sample sent to lab for NGS analysis; results available in 3-4 weeks.
Timeline: 3 to 4 Weeks
Patient Instructions
About This Test
Who Should Get This Test
To diagnose LCK Gene Immunodeficiency Type 22 by identifying mutations in the LCK gene using NGS technology, aiding in clinical management and genetic counseling.
How to Prepare
- Ensure proper identification
- Use sterile equipment
- Label samples correctly
- Store at ambient room temperature
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"This test is crucial for diagnosing LCK gene mutations causing immunodeficiency, enabling early treatment and genetic counseling for affected families."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed sample
- Insufficient volume
- Improperly labeled samples
Understanding Your Results
Pathogenic variant detected
Confirms diagnosis of LCK Gene Immunodeficiency Type 22; recommend clinical management and genetic counseling.
No pathogenic variant detected
LCK gene mutation unlikely; consider other causes of immunodeficiency.
Variant of uncertain significance
Further testing and family studies may be needed for clarification.
Consult a healthcare provider if experiencing recurrent infections, chronic diarrhea, failure to thrive, or if there is a family history of immunodeficiency disorders.
Limitations
- ⚠May not detect all possible mutations
- ⚠Requires genetic counseling for interpretation
- ⚠Results may have variants of uncertain significance
Risks & Considerations
- ●Minimal risks from blood draw, such as bruising or infection
- ●Psychological impact of genetic results
Interfering Factors
- ●Sample contamination
- ●Degraded DNA
- ●Improper sample storage
Compare With Similar Tests
| Test | LCK Gene Immunodeficiency type 22 NGS Genetic Test | Whole Exome Sequencing | Immunodeficiency Panel | Sanger Sequencing |
|---|---|---|---|---|
| Comparison | LCK Gene Immunodeficiency type 22 NGS Genetic Test |
Frequently Asked Questions
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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.
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✓ 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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