KEL Gene Hemolytic anemia, Kell-system related NGS Genetic Test
Short Name: KEL Gene Hemolytic Anemia Test
Also known as: Kell System Genetic Test, KEL Gene Mutation Analysis
KEL Gene Hemolytic anemia, Kell-system related 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 SULOCHANA HEMCHANDRA HOLLA
Consultant Medical Geneticist · Reg: 8532
Last reviewed: September 7, 2026
Overview
To diagnose KEL gene hemolytic anemia and other Kell-system related disorders by identifying mutations in the KEL gene using NGS technology.
- Test Code
- 5590
- 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
No special preparation required. Provide clinical history and family pedigree information.
Method: Venipuncture
Laboratory Analysis
Blood sample will be drawn by a trained phlebotomist using standard venipuncture techniques.
Report Delivery
Apply pressure to the puncture site to stop bleeding. Resume normal activities immediately.
Timeline: 3 to 4 weeks
Patient Instructions
About This Test
Who Should Get This Test
To diagnose KEL gene hemolytic anemia and other Kell-system related disorders by identifying mutations in the KEL gene using NGS technology.
How to Prepare
- Bring identification and doctor's prescription
- Inform about any medications or health conditions
- Ensure sample is properly labeled
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"This test is crucial for diagnosing hereditary hemolytic anemias and guiding family planning decisions."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed sample
- Insufficient volume
- Incorrect labeling or container
Understanding Your Results
Positive for pathogenic KEL gene mutation
Indicates diagnosis of KEL gene hemolytic anemia or related disorder; genetic counseling recommended
Negative for pathogenic mutations
No KEL gene mutations detected; symptoms may be due to other causes
Variant of uncertain significance
Further testing or family studies may be required for clarification
If symptoms persist, worsen, or if there is a family history of hemolytic anemia, consult a hematologist or geneticist.
Limitations
- ⚠May not detect all genetic variants
- ⚠Requires genetic counseling for accurate interpretation
Risks & Considerations
- ●Minimal physical risk from blood draw, such as bruising or infection
- ●Potential psychological impact of genetic results; genetic counseling recommended
Interfering Factors
- ●Sample degradation
- ●Contamination
- ●Incorrect sample type
Compare With Similar Tests
| Test | KEL Gene Hemolytic anemia, Kell-system related NGS Genetic Test | Complete Blood Count (CBC) | Direct Antiglobulin Test (DAT) | Single-gene sequencing |
|---|---|---|---|---|
| Comparison | KEL Gene Hemolytic anemia, Kell-system related NGS Genetic Test | CBC detects anemia but not genetic causes; NGS provides specific mutation analysis | DAT checks for antibodies on red blood cells; genetic test identifies underlying KEL gene mutations | NGS offers higher throughput and can detect multiple variants simultaneously |
Frequently Asked Questions
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