CLMP Gene Congenital short-bowel syndrome NGS Genetic Test
Short Name: CLMP Gene CSBS NGS Test
Also known as: CLMP-related CSBS Genetic Test, Congenital Short Bowel Syndrome DNA Test, CLMP Gene Mutation Analysis
CLMP Gene Congenital short-bowel syndrome NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses Next-Generation Sequencing (NGS), DNA Sequencing 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
The purpose of this test is to confirm a diagnosis of congenital short-bowel syndrome caused by CLMP gene mutations, identify genetic variants for family risk assessment, guide treatment and management strategies, and facilitate genetic counseling for inheritance patterns.
- Test Code
- 5726
- 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), DNA Sequencing
Sample Collection
Provide clinical history and undergo genetic counseling to draw a pedigree chart. No specific preparation is required, but ensure sample integrity.
Method: Blood Draw or Saliva Collection
Laboratory Analysis
A blood sample or saliva sample is collected by a trained phlebotomist. For blood, a venipuncture is performed; for saliva, a swab is used.
Report Delivery
Sample is labeled and transported to the lab under ambient room temperature. Results are available in 3 to 4 weeks.
Timeline: 3 to 4 Weeks
Patient Instructions
About This Test
Who Should Get This Test
The purpose of this test is to confirm a diagnosis of congenital short-bowel syndrome caused by CLMP gene mutations, identify genetic variants for family risk assessment, guide treatment and management strategies, and facilitate genetic counseling for inheritance patterns.
How to Prepare
- Use sterile collection tubes
- Label samples with patient details
- Avoid hemolysis during blood draw
- Store samples at room temperature if using FTA card
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"Early genetic testing for CLMP gene mutations can guide treatment decisions and family planning for congenital short-bowel syndrome."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed or clotted samples
- Insufficient sample volume
- Incorrect labeling or missing patient information
- Contaminated samples
Understanding Your Results
Positive for pathogenic variant
Confirms CLMP gene mutation associated with CSBS. Genetic counseling and management planning recommended.
Negative for pathogenic variant
No known mutations detected. Clinical correlation and further testing may be needed if symptoms persist.
Variant of uncertain significance (VUS)
Genetic variant identified but clinical significance unknown. Follow-up with genetic counselor advised.
Consult a healthcare provider if symptoms such as chronic diarrhea, vomiting, or weight loss persist, or for genetic counseling after receiving test results.
Limitations
- ⚠May not detect all types of genetic variants, such as large deletions or duplications
- ⚠Variants of uncertain significance (VUS) may be identified, requiring further evaluation
- ⚠Test results should be correlated with clinical presentation and family history
- ⚠Does not rule out other genetic or non-genetic causes of short-bowel syndrome
Risks & Considerations
- ●Minimal risks from blood draw, such as bruising or infection
- ●Psychological impact of genetic results; counseling provided
Interfering Factors
- ●Sample contamination
- ●Degraded DNA quality
- ●Hemolyzed or clotted blood samples
- ●Incorrect sample storage conditions
Compare With Similar Tests
| Test | CLMP Gene Congenital short-bowel syndrome NGS Genetic Test | CFTR Gene Test for Cystic Fibrosis | Hirschsprung Disease Genetic Test | Whole Exome Sequencing |
|---|---|---|---|---|
| Comparison | CLMP Gene Congenital short-bowel syndrome NGS Genetic Test | Focuses on different gene and condition; both are NGS-based but for distinct disorders. | Targets genes associated with Hirschsprung disease, another congenital digestive disorder. | Broader genetic analysis; CLMP test is targeted for specific gene mutations. |
Frequently Asked Questions
What is the CLMP Gene Congenital Short-Bowel Syndrome NGS Genetic Test?
What is the cost of this test?
How is the test performed?
What are the symptoms of CLMP gene-related CSBS?
Who should consider this test?
Is home sample collection available?
How long does it take to get results?
What does a positive result mean?
Is genetic counseling included?
Are there any risks associated with the test?
Can this test be used for prenatal diagnosis?
What should I do after receiving the results?
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₹20,000Reference 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.
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.
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