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
GM1-gangliosidosis, type I
GLB1
  • infantile form
Lysosomal Storage Diseases (LSDs)
GM1-gangliosidosis, type II
GLB1
  • Derry syndrome
  • juvenile form
Lysosomal Storage Diseases (LSDs)
GM1-gangliosidosis, type III
GLB1
  • adult form
Lysosomal Storage Diseases (LSDs)
GM2-gangliosidosis, AB variant
GM2A
  • GM2 activator deficiency
  • Tay-Sachs disease, AB variant
Lysosomal Storage Diseases (LSDs)
Galactosialidosis
CTSA
  • Combined deficiency of sialidase AND beta galactosidase
Lysosomal Storage Diseases (LSDs)
Gaucher disease, atypical, due to saposin C deficiency
PSAP
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)
Displaying entries 51 - 60 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