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
Fabry disease
GLA
  • Alpha-galactosidase A deficiency
Lysosomal Storage Diseases (LSDs)
Gaucher disease, type I
GBA
  • non-neuronopathic form
Lysosomal Storage Diseases (LSDs)
Gaucher disease, type II
GBA
Lysosomal Storage Diseases (LSDs)
Gaucher disease, type II, neuronopathic form, classic type
GBA
Lysosomal Storage Diseases (LSDs)
Gaucher disease, type II, perinatal lethal form
GBA
Lysosomal Storage Diseases (LSDs)
Gaucher disease, type III
GBA
  • neuronopathic form
Lysosomal Storage Diseases (LSDs)
Gaucher disease, type IIIC
GBA
  • neuronopathic form, cardiovascular form
Lysosomal Storage Diseases (LSDs)
Gaucher disease, atypical, due to saposin C deficiency
PSAP
Lysosomal Storage Diseases (LSDs)
Krabbe disease
GALC
  • Galactosylceramide beta-galactosidase deficiency
  • Globoid cell leukodystrophy
  • Krabbe leukodystrophy
  • Leukodystrophy, globoid cell
Lysosomal Storage Diseases (LSDs)
Krabbe disease, infantile form
GALC
Lysosomal Storage Diseases (LSDs)
Displaying entries 121 - 130 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