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 ▲
Farber Lipogranulomatosis
ASAH1
  • Acid Ceramidase Deficiency
Lysosomal Storage Diseases (LSDs)
Farber Lipogranulomatosis, type 1
ASAH1
Lysosomal Storage Diseases (LSDs)
Farber Lipogranulomatosis, type 2
ASAH1
Lysosomal Storage Diseases (LSDs)
Farber Lipogranulomatosis, type 3
ASAH1
Lysosomal Storage Diseases (LSDs)
Farber Lipogranulomatosis, type 4
ASAH1
Lysosomal Storage Diseases (LSDs)
Farber Lipogranulomatosis, type 5
ASAH1
Lysosomal Storage Diseases (LSDs)
POMT1/POMT2-CDG (cong. muscular dystrophy spectrum)
POMT1,POMT2
  • Muscular dystrophy-dystroglycanopathy (Congenital with brain and eye anomalies), type A, 1 (MDDGA1)
  • Muscular dystrophy-dystroglycanopathy (Congenital with brain and eye anomalies), type A, 2 (MDDGA2)
  • Walker-Warburg syndrome (WWS)
Congenital Disorders of Glycosylation (CDGs)
POMGNT1-CDG (cong. muscular dystrophy spectrum)
POMGNT1
  • Muscle-eye-brain disease (MEB)
  • Muscular dystrophy-dystroglycanopathy (Congenital with brain and eye anomalies), type A, 3 (MDDGA3)
Congenital Disorders of Glycosylation (CDGs)
Fukuyama congenital muscular dystrophy
FKTN
  • FKTN-CDG (cong. muscular dystrophy spectrum)
  • Fukuyama congenital muscular dystrophy (FCMD)
  • Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4 (MDDGA4)
Congenital Disorders of Glycosylation (CDGs)
SLC35D1-CDG
SLC35D1
  • Chondrodysplasia, lethal neonatal, with snail-like pelvis
  • Schneckenbecken dysplasia
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