GlyCosmos Portal

Glyco-Disease Genes Database (GDGDB)

GDGDB is a database of glycan-related diseases and their responsible genes.

Database	Last Updated
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Concept UI	Disease Name ▲	Gene Symbol	Disease Name Aliases	Disease Type	UniProt ID
CON00353	ALG1-CDG	ALG1	CDG-Ik Congenital disorder of glycosylation, type Ik	Congenital Disorders of Glycosylation (CDGs)	Q9BT22
CON00621	ALG11-CDG	ALG11	CDG-Ip Congenital Disorder of Glycosylation, Type Ip	Congenital Disorders of Glycosylation (CDGs)	Q2TAA5
CON00349	ALG12-CDG	ALG12	CDG-Ig Congenital disorder of glycosylation, type Ig	Congenital Disorders of Glycosylation (CDGs)	Q9BV10
CON00624	ALG13-CDG	ALG13	CDG-Is Congenital Disorder of Glycosylation, Type Is	Congenital Disorders of Glycosylation (CDGs)	Q9NP73
CON00351	ALG2-CDG	ALG2	CDG-Ii Congenital disorder of glycosylation, type Ii	Congenital Disorders of Glycosylation (CDGs)	Q9H553
CON00346	ALG3-CDG	ALG3	CDG-Id Congenital disorder of glycosylation, type Id	Congenital Disorders of Glycosylation (CDGs)	Q92685
CON00345	ALG6-CDG	ALG6	CDG-Ic Congenital disorder of glycosylation, type Ic	Congenital Disorders of Glycosylation (CDGs)	Q9Y672
CON00350	ALG8-CDG	ALG8	CDG-Ih Congenital disorder of glycosylation, type Ih	Congenital Disorders of Glycosylation (CDGs)	Q9BVK2
CON00354	ALG9-CDG	ALG9	CDG-IL Congenital disorder of glycosylation, type IL	Congenital Disorders of Glycosylation (CDGs)	Q9H6U8
CON00371	ATP6VOA2-CDG	ATP6V0A2	ATP6VOA2 defect (cutis laxa type II) Cutis laxa, autosomal recessive, type IIA (ARCL2A) Debre-Type cutis laxa V-ATPase a2 subunit defect	Congenital Disorders of Glycosylation (CDGs)	Q9Y487