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
Ehlers-Danlos syndrome, musculocontractural type
CHST14
  • Adducted thumb and clubfoot syndrome
Congenital Disorders of Glycosylation (CDGs)
Spondyloepiphyseal dysplasia with congenital joint dislocations
CHST3
  • Spondyloepiphyseal dysplasia, Omani type
Congenital Disorders of Glycosylation (CDGs)
Macular corneal dystrophy
CHST6
  • Macular corneal dystrophy Type I
  • Macular corneal dystrophy Type II
Congenital Disorders of Glycosylation (CDGs)
Temtamy preaxial brachydactyly syndrome
CHSY1
  • TPBS
Congenital Disorders of Glycosylation (CDGs)
COG1-CDG
COG1
  • CDG-IIg
  • CDGII/COG1 Cerebrocostomandibular-like syndrome
  • COG1 deficiency
  • Congenital disorder of glycosylation, type IIg
Congenital Disorders of Glycosylation (CDGs)
COG4-CDG
COG4
  • CDG-IIj
  • Congenital disorder of glycosylation, type IIj
Congenital Disorders of Glycosylation (CDGs)
COG5-CDG
COG5
  • CDG-IIi
  • Congenital disorder of glycosylation, type IIi
Congenital Disorders of Glycosylation (CDGs)
COG6-CDG
COG6
  • CDG-IIL
  • Congenital Disorder of Glycosylation, Type IIL
Congenital Disorders of Glycosylation (CDGs)
COG7-CDG
COG7
  • CDG-IIe
  • Congenital disorder of glycosylation, type IIe
Congenital Disorders of Glycosylation (CDGs)
COG8-CDG
COG8
  • CDG-IIh
  • COG8 deficiency
  • Congenital disorder of glycosylation, type IIh
Congenital Disorders of Glycosylation (CDGs)
Displaying entries 31 - 40 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