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	Disease IDs
CON00080	Metachromatic leukodystrophy	ARSA		Lysosomal Storage Diseases (LSDs)	P15289	DOID:10581
CON00629	Mental retardation, autosomal recessive 15	MAN1B1	MRT15	Congenital Disorders of Glycosylation (CDGs)	Q9UKM7
CON00630	Mental retardation, autosomal recessive 12	ST3GAL3	MRT12	Congenital Disorders of Glycosylation (CDGs)	Q11203
CON00042	Maroteaux-Lamy syndrome, severe form	ARSB		Lysosomal Storage Diseases (LSDs)	P15848
CON00043	Maroteaux-Lamy syndrome, mild form	ARSB		Lysosomal Storage Diseases (LSDs)	P15848
CON00044	Maroteaux-Lamy syndrome, intermediate form	ARSB		Lysosomal Storage Diseases (LSDs)	P15848
CON00391	Macular corneal dystrophy	CHST6	Macular corneal dystrophy Type I Macular corneal dystrophy Type II	Congenital Disorders of Glycosylation (CDGs)	Q9GZX3
CON00344	MPI-CDG	MPI	CDG-Ib Congenital disorder of glycosylation, type Ib Mannosephosphate isomerase deficiency Protein-losing enteropathy-hepatic fibrosis syndrome Saguenay-Lac Saint-Jean syndrome	Congenital Disorders of Glycosylation (CDGs)	P34949
CON00348	MPDU1-CDG	MPDU1	CDG-If Congenital disorder of glycosylation, type If	Congenital Disorders of Glycosylation (CDGs)	O75352
CON00358	MGAT2-CDG	MGAT2	CDG-IIa Congenital disorder of glycosylation, type IIa	Congenital Disorders of Glycosylation (CDGs)	Q10469