Disorders

ALG2-CDG (CDG-Ii)

Synonym(s): Carbohydrate-Deficient Glycoprotein Syndrome, Type Ii, CDG1i, CDGIi, Congenital Disorder of Glycosylation 1i, Congenital Disorder of Glycosylation Ii

OMIM

Gene	Locus	Protein
ALG2	9q31.1	Alpha-1,3-mannosyltransferase ALG2

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
Klinikum Stuttgart, Institute of Clinical Genetics - Stuttgart, Germany	• Sequence analysis of the entire coding region
PreventionGenetics, Clinical DNA Testing and DNA Banking - Marshfield, WI, USA	• Sequence analysis of the entire coding region • Deletion/duplication analysis

^* 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.