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
Pompe disease, infantile-onset form
GAA
Lysosomal Storage Diseases (LSDs)
Pompe disease, late-onset form
GAA
Lysosomal Storage Diseases (LSDs)
Galactosialidosis
CTSA
  • Combined deficiency of sialidase AND beta galactosidase
Lysosomal Storage Diseases (LSDs)
Duchenne muscular dystrophy
DMD
  • DMD
  • Muscular dystrophy, pseudohypertrophic progressive, Duchenne type
Congenital Disorders of Glycosylation (CDGs)
Metachromatic leukodystrophy
ARSA
Lysosomal Storage Diseases (LSDs)
Metachromatic leukodystrophy, infantile form
ARSA
Lysosomal Storage Diseases (LSDs)
Metachromatic leukodystrophy, juvenile form
ARSA
Lysosomal Storage Diseases (LSDs)
Metachromatic leukodystrophy, adult form
ARSA
Lysosomal Storage Diseases (LSDs)
B4GALT1-CDG
B4GALT1
  • CDG-IId
  • Congenital disorder of glycosylation, type IId
Congenital Disorders of Glycosylation (CDGs)
Sanfilippo syndrome D
GNS
  • MPS IIID
  • Mucopolysaccharidosis type IIID
Lysosomal Storage Diseases (LSDs)
Displaying entries 41 - 50 of 152 in total

International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01