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
CON00629	Mental retardation, autosomal recessive 15	MAN1B1	MRT15	Congenital Disorders of Glycosylation (CDGs)	Q9UKM7
CON00080	Metachromatic leukodystrophy	ARSA		Lysosomal Storage Diseases (LSDs)	P15289	DOID:10581
CON00083	Metachromatic leukodystrophy, adult form	ARSA		Lysosomal Storage Diseases (LSDs)	P15289	DOID:10581
CON00084	Metachromatic leukodystrophy, due to saposin B deficiency	PSAP	Sphingolipid activator protein 1 deficiency	Lysosomal Storage Diseases (LSDs)	P07602
CON00081	Metachromatic leukodystrophy, infantile form	ARSA		Lysosomal Storage Diseases (LSDs)	P15289	DOID:10581
CON00082	Metachromatic leukodystrophy, juvenile form	ARSA		Lysosomal Storage Diseases (LSDs)	P15289	DOID:10581
CON00039	Morquio syndrome A	GALNS	Galactosamine-6-sulphatase deficiency MPS IVA Morquio's syndrome, classic form Mucopolysaccharidosis type IVA	Lysosomal Storage Diseases (LSDs)	P34059	DOID:12804
CON00040	Morquio syndrome B	GLB1	MPS IVB Morquio-like syndrome Mucopolysaccharidosis type IVB	Lysosomal Storage Diseases (LSDs)	P16278	DOID:12804
CON00025	Mucolipidosis II (alpha/beta)	GNPTAB	I-cell disease ML-II N-Acetylglucosamine-1-phosphotransferase deficiency	Lysosomal Storage Diseases (LSDs)	Q3T906	DOID:3343
CON00026	Mucolipidosis III (alpha/beta)	GNPTAB	ML-III Pseudo-Hurler Polydystrophy	Lysosomal Storage Diseases (LSDs)	Q3T906	DOID:3343