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 Disease Name Aliases Disease Type ▲ UniProt ID Disease IDs
PMM2
  • CDG-Ia
  • Congenital disorder of glycosylation, type Ia
  • Jaeken syndrome
  • Phosphomannomutase 2 deficiency
Congenital Disorders of Glycosylation (CDGs)
  • C535739
  • MONDO:0008907
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)
  • C535740
  • MONDO:0011257
ALG6
  • CDG-Ic
  • Congenital disorder of glycosylation, type Ic
Congenital Disorders of Glycosylation (CDGs)
  • C535741
  • MONDO:0011291
ALG3
  • CDG-Id
  • Congenital disorder of glycosylation, type Id
Congenital Disorders of Glycosylation (CDGs)
  • C535742
  • MONDO:0010998
DPM1
  • CDG-Ie
  • Congenital disorder of glycosylation, type Ie
Congenital Disorders of Glycosylation (CDGs)
  • C535743
  • MONDO:0012123
MPDU1
  • CDG-If
  • Congenital disorder of glycosylation, type If
Congenital Disorders of Glycosylation (CDGs)
  • C535744
  • MONDO:0012211
ALG12
  • CDG-Ig
  • Congenital disorder of glycosylation, type Ig
Congenital Disorders of Glycosylation (CDGs)
  • C535745
  • MONDO:0011783
ALG8
  • CDG-Ih
  • Congenital disorder of glycosylation, type Ih
Congenital Disorders of Glycosylation (CDGs)
  • C535746
  • MONDO:0011969
ALG2
  • CDG-Ii
  • Congenital disorder of glycosylation, type Ii
Congenital Disorders of Glycosylation (CDGs)
  • C535747
  • MONDO:0005501
DPAGT1
  • CDG-Ij
  • Congenital disorder of glycosylation, type Ij
Congenital Disorders of Glycosylation (CDGs)
  • C535748
  • MONDO:0011964
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