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
Tay-Sachs disease, late-onset forms
HEXA
  • Juvenile/Chronic/Adult-onset
Lysosomal Storage Diseases (LSDs)
Gaucher disease, atypical, due to saposin C deficiency
PSAP
Lysosomal Storage Diseases (LSDs)
Metachromatic leukodystrophy, due to saposin B deficiency
PSAP
  • Sphingolipid activator protein 1 deficiency
Lysosomal Storage Diseases (LSDs)
Combined saposin deficiency
PSAP
  • prosaposin deficiency
  • saposin deficiency
Lysosomal Storage Diseases (LSDs)
Sandhoff disease
HEXB
  • GM2-gangliosidosis, type II
Lysosomal Storage Diseases (LSDs)
Sandhoff disease, infantile form
HEXB
Lysosomal Storage Diseases (LSDs)
Sandhoff disease, juvenile form
HEXB
Lysosomal Storage Diseases (LSDs)
Sandhoff disease, adult form
HEXB
Lysosomal Storage Diseases (LSDs)
Mucopolysaccharidosis VII
GUSB
  • MPS VII
  • Sly syndrome
Lysosomal Storage Diseases (LSDs)
Pompe disease
GAA
  • GSD type II
  • Lysosomal alpha 1,4 Glucosidase Deficiency Disease
Lysosomal Storage Diseases (LSDs)
Displaying entries 31 - 40 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