Otogenetics Hearing Loss and Deafness Multi-Gene NGS Panel
- GTR Test IDHelpEach Test is a specific, orderable test from a particular laboratory, and is assigned a unique GTR accession number. The format is GTR00000001.1, with a leading prefix 'GTR' followed by 8 digits, a period, then 1 or more digits representing the version. When a laboratory updates a registered test, a new version number is assigned.: GTR000552366.2
- Last updated: 2022-04-15
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- Test version history
Clinical testHelpIn the U.S., clinical tests must be performed under CLIA certification. When a lab uses the same methods for a test in both clinical and research settings, the test appears as two separate GTR records. for Alagille syndrome due to a JAG1 point mutation
Offered by Otogenetics
Overview
Test name
HelpThe name the laboratory assigns the test. Used as the default title of the page specific to the test.Otogenetics Hearing Loss and Deafness Multi-Gene NGS Panel (Otogenetics Deafness Panel)
This is a clinical test intended for HelpPurposes or indications for the test. Lab-provided.: Diagnosis, Monitoring, Risk Assessment, Therapeutic management
Click Indication tab for more information.
Download and complete Test Requisition form and submit with specimen.
Order URL HelpLink to the laboratory webpage with information about how to order this test. Please note that clicking on this link will open a new tab in your internet browser.: http://www.otogenetics.com/genepanels/deafness-gene-panel-GTR.pdf
Specimen source
Methodology
HelpThe assay's major method category (biochemical, cytogenetic or molecular genetics); method category (i.e. enzyme assay, chromosome breakage studies, targeted mutation analysis); methodology (i.e. the name of the method used) and instruments used when performing this test.- Molecular Genetics
- ESequence analysis of select exons
- Next-Generation (NGS)/Massively parallel sequencing (MPS)
- Illumina HiSeq 2500
Establish or confirm diagnosis
- Genetic and clinical analysis of nonsyndromic hearing impairment in pediatric and adult cases. - PubMed ID: 27785406
Clinical validity
HelpHow consistently and accurately the test detects or predicts the intermediate or final outcomes of interest. Lab-provided.Not provided
Test services
HelpLaboratory's order or catalog code for the test (used in the order requisition form).- Clinical Testing/Confirmation of Mutations Identified Previously, Order code: oto-da3-gtr
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