Lysosomal Disorders 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.: GTR000509436.12
- Last updated: 2023-08-22
- Test version history
- 509436.12, last updated: 2023-08-22
- 509436.11, last updated: 2019-03-20
- 509436.10, last updated: 2017-08-25
- 509436.9, last updated: 2016-05-13
- 509436.8, last updated: 2015-09-01
- 509436.7, last updated: 2014-12-15
- 509436.6, last updated: 2014-07-02
- 509436.5, last updated: 2014-06-17
- 509436.4, last updated: 2014-06-13
- 509436.3, last updated: 2014-05-30
- 509436.2, last updated: 2014-04-03
- 509436.1, last updated: 2014-04-03
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 Type II diabetes mellitus
Offered by Fulgent Genetics
- NICE, 2023UK NICE Guidance, Clinical Guideline CG181, Cardiovascular disease: risk assessment and reduction, including lipid modification, 2023
- NICE, 2022UK NICE Guideline NG18, Diabetes (type 1 and type 2) in children and young people: diagnosis and management
- NICE, 2022UK NICE Guideline NG28, Type 2 diabetes in adults: management, 2022
- NICE, 2022UK NICE Guideline NG136, Hypertension in adults: diagnosis and management, 2022
- NICE, 2020UK NICE Guideline NG3, Diabetes in pregnancy: management from preconception to the postnatal period
- NICE, 2019UK NICE Guideline NG19, Diabetic foot problems: prevention and management, 2019
- OMIM
- View AKT2 variations in ClinVar
- View GCK variations in ClinVar
- View GPD2 variations in ClinVar
- View HMGA1 variations in ClinVar
- View HNF4A variations in ClinVar
- View IL6 variations in ClinVar
- View PDX1 variations in ClinVar
- View IRS1 variations in ClinVar
- View KCNJ11 variations in ClinVar
- View LIPC variations in ClinVar
- View MTNR1B variations in ClinVar
- View NEUROD1 variations in ClinVar
- View PAX4 variations in ClinVar
- View ENPP1 variations in ClinVar
- View PPARG variations in ClinVar
- View PPP1R3A variations in ClinVar
- View PTPN1 variations in ClinVar
- View SLC2A2 variations in ClinVar
- View ABCC8 variations in ClinVar
- View HNF1A variations in ClinVar
- View HNF1B variations in ClinVar
- View TCF7L2 variations in ClinVar
- View WFS1 variations in ClinVar
- View IRS2 variations in ClinVar
- View MAPK8IP1 variations in ClinVar
- View IGF2BP2 variations in ClinVar
- View RETN variations in ClinVar
- View SLC30A8 variations in ClinVar
- RefSeqGene
- Coriell Institute for Medical Research
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.