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SLC6A14 Gene Cystic fibrosis, SLC6A14 related NGS Genetic Test

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SLC6A14 Gene Cystic fibrosis, SLC6A14 related NGS Genetic Test

Short Name: SLC6A14 Gene Cystic Fibrosis NGS Test

Also known as: SLC6A14 mutation test, CF genetic test with SLC6A14, SLC6A14-related CF test

SLC6A14 Gene Cystic fibrosis, SLC6A14 related 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 Reports are typically available within 3 to 4 weeks from sample receipt.. Free home collection in 300+ cities across India.

NGS Genetic Test🏠 Home Collection

🩺 Medically Reviewed By

Overview

To detect mutations in the SLC6A14 gene that may modify cystic fibrosis symptoms, aiding in early diagnosis, risk assessment, and personalized treatment planning.

Test Code
1964
Price
₹20,000
Sample Type
Blood or Extracted DNA or One drop Blood on FTA Card
Result Time
Reports are typically available within 3 to 4 weeks from sample receipt.
Fasting Required
No
Method
NGS Technology
Step 1

Sample Collection

Provide detailed clinical history of the patient and undergo a genetic counseling session to draw a pedigree chart of family members affected with cystic fibrosis or related disorders.

Method: Venipuncture or FTA card application

Step 2

Laboratory Analysis

A blood sample is drawn from a vein using standard venipuncture, or a drop of blood is applied to an FTA card under aseptic conditions.

Step 3

Report Delivery

The sample is labeled, stored at ambient room temperature, and transported to the laboratory for DNA extraction and NGS analysis.

Timeline: Reports are typically available within 3 to 4 weeks from sample receipt.

Patient Instructions

1
Before the Test:Genetic counseling is required to discuss test implications, obtain informed consent, and gather family history details.
2
During the Test:Sample collection involves a simple blood draw or FTA card application, followed by laboratory-based NGS analysis.
3
After the Test:A detailed clinical report is generated, and genetic counseling is provided to explain results and next steps.

About This Test

Who Should Get This Test

To detect mutations in the SLC6A14 gene that may modify cystic fibrosis symptoms, aiding in early diagnosis, risk assessment, and personalized treatment planning.

How to Prepare

  • Ensure proper patient identification and labeling
  • Use sterile equipment for blood draw
  • Apply blood to FTA card as per instructions
  • Transport samples at ambient temperature without refrigeration

Doctor's Notes

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

"Identifying SLC6A14 mutations can provide insights into cystic fibrosis variability and guide personalized treatment strategies."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Sample Volume5 ml blood
ContainerEDTA tube or FTA card
Collection MethodVenipuncture or FTA card application

Sample Stability

Blood sample: Stable at 4°C for up to 7 days
FTA card: Stable at room temperature for extended periods if stored correctly
Sample Rejection Criteria:
  • Hemolyzed or clotted blood samples
  • Insufficient sample volume
  • Contaminated or mislabeled samples
  • Incorrect sample type for the requested test

Understanding Your Results

Test results indicate the presence or absence of pathogenic mutations in the SLC6A14 gene. Results should be interpreted in conjunction with clinical findings and family history.
📊

Positive

Pathogenic variants detected in SLC6A14 gene, which may increase cystic fibrosis risk or modify symptoms. Genetic counseling recommended.

📊

Negative

No pathogenic variants detected in SLC6A14 gene. However, this does not rule out cystic fibrosis if CFTR mutations are present.

📊

Variant of Uncertain Significance

Genetic change identified, but its clinical impact is unknown. Further testing or family studies may be advised.

⚠️ When to Consult a Doctor:

Consult a geneticist or pulmonologist if mutations are detected, if symptoms persist despite negative results, or for personalized management of cystic fibrosis.

Limitations

  • Not all genetic variants may be detected due to technical limitations
  • Results do not confirm clinical diagnosis alone and require correlation with symptoms
  • Variant of uncertain significance (VUS) may require further investigation

Risks & Considerations

  • Minimal risk from blood draw: bruising, soreness, or infection at the collection site
  • No risk from FTA card collection method
  • Psychological impact from test results, mitigated through genetic counseling

Interfering Factors

  • Contaminated or degraded DNA sample
  • Incorrect sample type or collection method
  • Hemolyzed blood samples
  • Recent blood transfusions may affect results

Compare With Similar Tests

TestSLC6A14 Gene Cystic fibrosis, SLC6A14 related NGS Genetic TestCFTR Gene Mutation TestSweat Chloride TestLung Function TestsChest CT Scan
ComparisonSLC6A14 Gene Cystic fibrosis, SLC6A14 related NGS Genetic Test

Frequently Asked Questions

What is the SLC6A14 gene?
The SLC6A14 gene encodes a sodium-dependent neutral amino acid transporter protein located on chromosome 4q28.3. It is involved in amino acid transport and has been linked to cystic fibrosis as a modifier gene.
How is SLC6A14 related to cystic fibrosis?
Research indicates that mutations in SLC6A14 may act as modifiers of CFTR function, potentially contributing to the development or severity of cystic fibrosis in some individuals.
What are the symptoms of cystic fibrosis?
Common symptoms include chronic coughing, wheezing or shortness of breath, frequent lung infections, poor growth or weight gain in children, and frequent greasy or bulky stools.
How is cystic fibrosis diagnosed?
Diagnosis typically involves a combination of sweat chloride tests, genetic testing, lung function tests, and imaging such as chest X-rays or CT scans.
What is NGS genetic testing?
Next-generation sequencing (NGS) is a DNA sequencing technology that allows for rapid, accurate analysis of multiple genes or large genomic regions, used for detecting inherited mutations.
What is the cost of the SLC6A14 gene test in India?
The cost is approximately INR 20000, including home sample collection across India.
How long does it take to get results?
Results are typically available within 3 to 4 weeks from sample collection.
Is home sample collection available?
Yes, free home sample collection is offered for online bookings in numerous cities across India.
What sample is required for this test?
The test requires blood, extracted DNA, or one drop of blood on an FTA card.
Who should consider this test?
Individuals with family history of cystic fibrosis, chronic respiratory or digestive symptoms suggestive of CF, or those seeking genetic counseling for CF risk assessment.
What does a positive result mean?
A positive result indicates the presence of pathogenic mutations in the SLC6A14 gene, which may increase cystic fibrosis risk or modify symptoms. Genetic counseling is recommended.
Are there any risks associated with this test?
Risks are minimal, primarily related to blood draw such as bruising or soreness. Psychological impacts are mitigated through genetic counseling sessions included with the test.
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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For Hospitals & Clinics

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.

LIMS Integration

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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