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
Combined saposin deficiency
PSAP
  • prosaposin deficiency
  • saposin deficiency
Lysosomal Storage Diseases (LSDs)
Gaucher disease, type I
GBA
  • non-neuronopathic form
Lysosomal Storage Diseases (LSDs)
Niemann-Pick disease, type B
SMPD1
  • non-neurological type
Lysosomal Storage Diseases (LSDs)
Gaucher disease, type IIIC
GBA
  • neuronopathic form, cardiovascular form
Lysosomal Storage Diseases (LSDs)
Gaucher disease, type III
GBA
  • neuronopathic form
Lysosomal Storage Diseases (LSDs)
Niemann-Pick disease, type A
SMPD1
  • neurological type
Lysosomal Storage Diseases (LSDs)
Schindler disease, type I
NAGA
  • infantile type
Lysosomal Storage Diseases (LSDs)
GM1-gangliosidosis, type I
GLB1
  • infantile form
Lysosomal Storage Diseases (LSDs)
GM1-gangliosidosis, type III
GLB1
  • adult form
Lysosomal Storage Diseases (LSDs)
GALNT3-CDG
GALNT3
  • Tumoral calcinosis, hyperphosphatemic, familial
Congenital Disorders of Glycosylation (CDGs)
Displaying entries 1 - 10 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