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
MPI-CDG
MPI
  • CDG-Ib
  • Congenital disorder of glycosylation, type Ib
  • Mannosephosphate isomerase deficiency
  • Protein-losing enteropathy-hepatic fibrosis syndrome
  • Saguenay-Lac Saint-Jean syndrome
Congenital Disorders of Glycosylation (CDGs)
ALG6-CDG
ALG6
  • CDG-Ic
  • Congenital disorder of glycosylation, type Ic
Congenital Disorders of Glycosylation (CDGs)
ALG3-CDG
ALG3
  • CDG-Id
  • Congenital disorder of glycosylation, type Id
Congenital Disorders of Glycosylation (CDGs)
DPM1-CDG
DPM1
  • CDG-Ie
  • Congenital disorder of glycosylation, type Ie
Congenital Disorders of Glycosylation (CDGs)
MPDU1-CDG
MPDU1
  • CDG-If
  • Congenital disorder of glycosylation, type If
Congenital Disorders of Glycosylation (CDGs)
ALG12-CDG
ALG12
  • CDG-Ig
  • Congenital disorder of glycosylation, type Ig
Congenital Disorders of Glycosylation (CDGs)
ALG8-CDG
ALG8
  • CDG-Ih
  • Congenital disorder of glycosylation, type Ih
Congenital Disorders of Glycosylation (CDGs)
ALG2-CDG
ALG2
  • CDG-Ii
  • Congenital disorder of glycosylation, type Ii
Congenital Disorders of Glycosylation (CDGs)
DPAGT1-CDG
DPAGT1
  • CDG-Ij
  • Congenital disorder of glycosylation, type Ij
Congenital Disorders of Glycosylation (CDGs)
ALG1-CDG
ALG1
  • CDG-Ik
  • Congenital disorder of glycosylation, type Ik
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