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
Disease Name Gene Symbol Alias Disease Names Disease Type UniProt ID Disease IDs
GLB1
  • Derry syndrome
  • juvenile form
Lysosomal Storage Diseases (LSDs)
  • DOID:3322
  • MESH:D016537
  • MONDO:0018149
MAN2B1
Lysosomal Storage Diseases (LSDs)
  • DOID:3413
  • MESH:D008363
  • MONDO:0009561
MAN2B1
Lysosomal Storage Diseases (LSDs)
  • DOID:3413
  • MESH:D008363
  • MONDO:0009561
SUMF1
  • MSD
  • Multiple sulfatase deficiency disease
Lysosomal Storage Diseases (LSDs)
  • MESH:D052517
  • MONDO:0010088
GAA
Lysosomal Storage Diseases (LSDs)
  • DOID:2752
  • MESH:D006009
PLOD1
  • Ehlers-Danlos syndrome, kyphoscoliotic type
  • Nevo syndrome
Congenital Disorders of Glycosylation (CDGs)
  • DOID:14775
  • MESH:C536198
SLC26A2
  • Diastrophic dwarfism
Congenital Disorders of Glycosylation (CDGs)
  • DOID:14687
  • MESH:C536170
  • MONDO:0009107
FKTN
  • FKTN-CDG (cong. muscular dystrophy spectrum)
  • Limb-girdle muscular dystrophy type 2M (LGMD2M)
  • Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 4 (MDDGC4)
Congenital Disorders of Glycosylation (CDGs)
  • MESH:C566912
  • MONDO:0012699
GNE
  • GNE-CDG (hereditary inclusion body myopathy)
  • Hereditary inclusion body myopathy type 2 (HIBM2)
  • Inclusion body myopathy 2, autosomal recessive (IBM2)
Congenital Disorders of Glycosylation (CDGs)
  • MESH:C538329
GAA
Lysosomal Storage Diseases (LSDs)
  • DOID:2752
  • MESH:D006009
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