SLC35A1 Gene Glycosylation disorder type 2F NGS Genetic Test
Short Name: SLC35A1 Gene Test
Also known as: Congenital Disorder of Glycosylation Type 2F, CDG Type 2F
SLC35A1 Gene Glycosylation disorder type 2F 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 Pasupathy Arumugam
Consultant Pathologist · Reg: 21521
Last reviewed: September 3, 2026
Overview
To identify mutations in the SLC35A1 gene associated with Glycosylation Disorder Type 2F, aiding in accurate diagnosis and management of the condition.
- Test Code
- 4689
- 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
Ensure genetic counseling is completed and clinical history is provided.
Laboratory Analysis
Blood sample will be collected via venipuncture or using FTA card for one drop blood.
Report Delivery
Apply pressure to the puncture site to prevent bruising. Store sample as instructed.
Timeline: 3 to 4 weeks
Patient Instructions
About This Test
Who Should Get This Test
To identify mutations in the SLC35A1 gene associated with Glycosylation Disorder Type 2F, aiding in accurate diagnosis and management of the condition.
How to Prepare
- Fast for 8-12 hours if required, but typically not needed for genetic tests
- Bring identification and prescription
- Inform about any medications
Doctor's Notes
Reviewed by Dr Pasupathy Arumugam — MBBS, MD (Pathology) · Reg. No. 21521
"This NGS genetic test is essential for diagnosing SLC35A1-related glycosylation disorders, enabling early intervention and family planning."
Last medically reviewed: September 3, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed sample
- Insufficient volume
- Incorrect labeling
Understanding Your Results
Pathogenic variant detected
Confirms diagnosis of Glycosylation Disorder Type 2F
No pathogenic variant detected
Condition unlikely, but clinical correlation is needed
Variant of uncertain significance
Further testing and family studies may be required
If symptoms of glycosylation disorder are present, or if family history suggests genetic risk.
Limitations
- ⚠May not detect all genetic variants
- ⚠Requires interpretation by a geneticist
- ⚠Not a standalone diagnostic tool
Risks & Considerations
- ●Minimal risk from blood draw
- ●Possible bruising or infection at puncture site
Interfering Factors
- ●Sample contamination
- ●Degraded DNA
- ●Incorrect sample type
Compare With Similar Tests
| Test | SLC35A1 Gene Glycosylation disorder type 2F NGS Genetic Test | Whole Exome Sequencing | Targeted Gene Panel |
|---|---|---|---|
| Comparison | SLC35A1 Gene Glycosylation disorder type 2F NGS Genetic Test |
Frequently Asked Questions
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