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
TMEM15
  • CDG-Im
  • Congenital disorder of glycosylation, type Im
  • DK1 deficiency
  • DK1-CDG
  • Dolichol kinase deficiency
Congenital Disorders of Glycosylation (CDGs)
  • C563666
  • MONDO:0012556
DPAGT1
  • CDG-Ij
  • Congenital disorder of glycosylation, type Ij
Congenital Disorders of Glycosylation (CDGs)
  • C535748
  • MONDO:0011964
DPM1
  • CDG-Ie
  • Congenital disorder of glycosylation, type Ie
Congenital Disorders of Glycosylation (CDGs)
  • C535743
  • MONDO:0012123
DPM3
  • CDG-Io
  • Congenital Disorder of Glycosylation, Type Io
Congenital Disorders of Glycosylation (CDGs)
  • C567857
  • MONDO:0013049
SLC26A2
  • Diastrophic dwarfism
Congenital Disorders of Glycosylation (CDGs)
  • C536170
  • DOID:14687
  • MONDO:0009107
DMD
  • DMD
  • Muscular dystrophy, pseudohypertrophic progressive, Duchenne type
Congenital Disorders of Glycosylation (CDGs)
  • D020388
  • DOID:11723
  • MONDO:0010679
EXT1,EXT2
  • Exostoses, multiple, type 1
  • Exostoses, multiple, type 2
  • Hereditary multiple exostoses (HME)
  • Hereditary multiple osteochondromas (HMO)
  • Multiple cartilaginous exostoses
Congenital Disorders of Glycosylation (CDGs)
  • C538356
  • D005097
  • DOID:206
  • MONDO:0005508
  • MONDO:0011022
CHST14
  • Adducted thumb and clubfoot syndrome
Congenital Disorders of Glycosylation (CDGs)
  • C538226
PLOD1
  • Ehlers-Danlos syndrome, kyphoscoliotic type
  • Nevo syndrome
Congenital Disorders of Glycosylation (CDGs)
  • C536198
  • DOID:14775
GLA
  • Alpha-galactosidase A deficiency
Lysosomal Storage Diseases (LSDs)
  • D000795
  • DOID:14499
  • MONDO:0010526
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