Disorders

ALG9-CDG (CDG-IL)

Synonym(s): Carbohydrate-Deficient Glycoprotein Syndrome, Type Il, CDG1l, CDGIl, Congenital Disorder of Glycosylation 1L, Congenital Disorder of Glycosylation IL

OMIM

Gene	Locus	Protein
ALG9	11q23	Alpha-1,2-mannosyltransferase ALG9

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

^* 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.