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
GALNT3-CDG
GALNT3
  • Tumoral calcinosis, hyperphosphatemic, familial
Congenital Disorders of Glycosylation (CDGs)
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)
GCS1-CDG
GCS1
  • CDG-IIb
  • Congenital disorder of glycosylation, type IIb
  • MOGS-CDG
Congenital Disorders of Glycosylation (CDGs)
Myasthenia, congenital, with tubular aggregates 1
GFPT1
  • CMSTA1
Congenital Disorders of Glycosylation (CDGs)
Fabry disease
GLA
  • Alpha-galactosidase A deficiency
Lysosomal Storage Diseases (LSDs)
Displaying entries 61 - 70 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