Disorders


 

DPAGT1-CDG (CDG-Ij)


Synonym(s): Carbohydrate-Deficient Glycoprotein Syndrome, Type Ij, CDG1j, CDGIj, Congenital Disorder of Glycosylation 1j, Congenital Disorder of Glycosylation Ij

 

OMIM

GeneLocusProtein
DPAGT111q23.3UDP-N-acetylglucosamine--dolichyl-phosphate N-acetylglucosaminephosphotransferase

Laboratory Test Method Prenatal Carrier *
Centogene AG, Rare Disease Company - Rostock, Germany• Sequence analysis of the entire coding region
Emory University School of Medicine, Emory Molecular Genetics Laboratory - Atlanta, GA, USA• Sequence analysis of the entire coding region
• Deletion/duplication analysis
Universidad Autonoma de Madrid, Centro de Diagnostico de Enfermedades Moleculares - Madrid, Spain• Sequence analysis of the entire coding region
• Analyte

* Carrier column is relevant to autosomal recessive and X-linked inheritance; column will be blank when it is not relevant (e.g. autosomal dominant inheritance, microdeletions/duplications) and/or is not offered by the lab.

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