ALG11 Gene Congenital disorder of glycosylation, type Ip NGS Genetic DNA Test
- 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.: GTR000607451.1
- Last updated: 2023-04-27
- Test version history
- 607451.1, last updated: 2023-04-27
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 Hereditary disease
Offered by DNA Labs India
Overview
Test name
HelpThe name the laboratory assigns the test. Used as the default title of the page specific to the test.ALG11 Gene Congenital disorder of glycosylation, type Ip NGS Genetic DNA Test (ALG11 Gene Congenital disorder of glycosylation, type Ip NGS Gen)
This is a clinical test intended for HelpPurposes or indications for the test. Lab-provided.: Screening
Click Indication tab for more information.
Just place order online with doctor prescription
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.: https://dnalabsindia.com/test/alg11-gene-congenital-disorder-of-glycosylation-type-ip-ngs-genetic-dna-test
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
- SMutation scanning of the entire coding region
- Next-Generation (NGS)/Massively parallel sequencing (MPS)
- Illumina HiSeq™2000 system
Not provided
Clinical validity
HelpHow consistently and accurately the test detects or predicts the intermediate or final outcomes of interest. Lab-provided.This panel should be performed in all individuals suspected of having an overlapping clinical phenotype. Confirmation of a clinical diagnosis through genetic testing can allow for genetic counseling and may direct medical management. Genetic counseling can provide a patient and/or family with the natural history of the condition, identify at-risk family members, provide reproductive risks as well as preconception/prenatal options, and allow for appropriate referral for patient support and/or resources.
Citations
Not provided
- AAP, 2013Ethical and Policy Issues in Genetic Testing and Screening of Children, Pediatrics (2013) 131 (3): 620–622.
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.