Pan Cardiomyopathy Panel (51 Genes)
- 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.: GTR000509149.2
- Last updated: 2014-12-10
- Test version history
- 509149.12, last updated: 2023-12-04
- 509149.11, last updated: 2022-09-06
- 509149.10, last updated: 2021-09-08
- 509149.9, last updated: 2020-01-15
- 509149.8, last updated: 2019-11-01
- 509149.7, last updated: 2018-11-30
- 509149.6, last updated: 2017-11-09
- 509149.5, last updated: 2016-11-10
- 509149.4, last updated: 2015-11-23
- 509149.3, last updated: 2015-02-17
- 509149.2, last updated: 2014-12-10
- 509149.1, last updated: 2013-12-13
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 Primary dilated cardiomyopathy
Offered by Laboratory for Molecular Medicine
Overview
Test name
HelpThe name the laboratory assigns the test. Used as the default title of the page specific to the test.Pan Cardiomyopathy Panel (51 Genes)
This is a clinical test intended for HelpPurposes or indications for the test. Lab-provided.: Diagnosis
Click Indication tab for more information.
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://personalizedmedicine.partners.org/Laboratory-For-Molecular-Medicine/Ordering/Cardiomyopathy/PanCardiomyopathy-Panel.aspx
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
- DDeletion/duplication analysis
- Other
- CSequence analysis of the entire coding region
- Next-Generation (NGS)/Massively parallel sequencing (MPS)
Not provided
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
- OMIM
- View ACTC1 variations in ClinVar
- View ACTN2 variations in ClinVar
- View DES variations in ClinVar
- View DSG2 variations in ClinVar
- View EYA4 variations in ClinVar
- View FKTN variations in ClinVar
- View LMNA variations in ClinVar
- View MYBPC3 variations in ClinVar
- View MYH6 variations in ClinVar
- View PLN variations in ClinVar
- View PSEN1 variations in ClinVar
- View PSEN2 variations in ClinVar
- View SGCD variations in ClinVar
- View TAFAZZIN variations in ClinVar
- View TMPO variations in ClinVar
- View TNNT2 variations in ClinVar
- View TPM1 variations in ClinVar
- View TTN variations in ClinVar
- View VCL variations in ClinVar
- View CSRP3 variations in ClinVar
- View TCAP variations in ClinVar
- View BAG3 variations in ClinVar
- View ABCC9 variations in ClinVar
- View LDB3 variations in ClinVar
- View ANKRD1 variations in ClinVar
- View NEXN variations in ClinVar
- View RBM20 variations in ClinVar
- RefSeqGene
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.