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 ▲
CON00015	Sialidosis type II, congenital form	NEU1		Lysosomal Storage Diseases (LSDs)	Q99519
CON00016	Sialidosis type II, infantile form	NEU1		Lysosomal Storage Diseases (LSDs)	Q99519
CON00017	Sialidosis type II, juvenile form	NEU1		Lysosomal Storage Diseases (LSDs)	Q99519
CON00353	ALG1-CDG	ALG1	CDG-Ik Congenital disorder of glycosylation, type Ik	Congenital Disorders of Glycosylation (CDGs)	Q9BT22
CON00349	ALG12-CDG	ALG12	CDG-Ig Congenital disorder of glycosylation, type Ig	Congenital Disorders of Glycosylation (CDGs)	Q9BV10
CON00350	ALG8-CDG	ALG8	CDG-Ih Congenital disorder of glycosylation, type Ih	Congenital Disorders of Glycosylation (CDGs)	Q9BVK2
CON00391	Macular corneal dystrophy	CHST6	Macular corneal dystrophy Type I Macular corneal dystrophy Type II	Congenital Disorders of Glycosylation (CDGs)	Q9GZX3
CON00352	DPAGT1-CDG	DPAGT1	CDG-Ij Congenital disorder of glycosylation, type Ij	Congenital Disorders of Glycosylation (CDGs)	Q9H3H5
CON00415	PIGM-CDG	PIGM	Autosomal recessive GPI anchor deficiency Glycosylphosphatidylinositol deficiency	Congenital Disorders of Glycosylation (CDGs)	Q9H3S5
CON00351	ALG2-CDG	ALG2	CDG-Ii Congenital disorder of glycosylation, type Ii	Congenital Disorders of Glycosylation (CDGs)	Q9H553