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GTR Home > Tests > JAG1 Sequencing

Overview

Test name

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JAG1 Sequencing (JAG1)

Purpose of the test

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This is a clinical test intended for Help: Diagnosis, Mutation Confirmation, Pre-symptomatic, Risk Assessment

Condition

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Click Indication tab for more information.

How to order

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Complete the appropriate test requisition and have it signed by the referring physician.
Order URL Help: http://www.cincinnatichildrens.org/service/d/diagnostic-labs/molecular-genetics/requisition/

Methodology

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Molecular Genetics
CSequence analysis of the entire coding region
Bi-directional Sanger Sequence Analysis
TTargeted variant analysis
Bi-directional Sanger Sequence Analysis

Summary of what is tested

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Click Methodology tab for more information.

Clinical utility

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Not provided

Clinical validity

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Not provided

Testing strategy

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JAG1 genetic testing is also available as part of our JaundiceChip Resequencing Array. If Alagille syndrome is suspected, full sequencing of JAG1 is recommended instead of JaundiceChip. 000 Complete the appropriate test requisition and have it signed by the referring physician.

Test services

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  • Clinical Testing/Confirmation of Mutations Identified Previously
  • Custom Prenatal Testing
  • Custom mutation-specific/Carrier testing

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.