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
Schindler disease, type II
NAGA
  • Kanzaki disease
Lysosomal Storage Diseases (LSDs)
B3GALTL-CDG
B3GALTL
  • Krause-Kivlin syndrome
  • Peters anomaly with short limb dwarfism
  • Peters-plus syndrome
Congenital Disorders of Glycosylation (CDGs)
Multiple congenital anomalies-hypotonia-seizures syndrome 1
PIGN
  • MCAHS1
Congenital Disorders of Glycosylation (CDGs)
Mucolipidosis III (alpha/beta)
GNPTAB
  • ML-III
  • Pseudo-Hurler Polydystrophy
Lysosomal Storage Diseases (LSDs)
Sanfilippo syndrome A
SGSH
  • MPS IIIA
  • Mucopolysaccharidosis type IIIA
Lysosomal Storage Diseases (LSDs)
Sanfilippo syndrome B
NAGLU
  • MPS IIIB
  • Mucopolysaccharidosis type IIIB
Lysosomal Storage Diseases (LSDs)
Sanfilippo syndrome C
HGSNAT
  • MPS IIIC
  • Mucopolysaccharidosis type IIIC
Lysosomal Storage Diseases (LSDs)
Sanfilippo syndrome D
GNS
  • MPS IIID
  • Mucopolysaccharidosis type IIID
Lysosomal Storage Diseases (LSDs)
Morquio syndrome B
GLB1
  • MPS IVB
  • Morquio-like syndrome
  • Mucopolysaccharidosis type IVB
Lysosomal Storage Diseases (LSDs)
Mucopolysaccharidosis VI
ARSB
  • MPS VI, Maroteaux-Lamy syndrome
Lysosomal Storage Diseases (LSDs)
Displaying entries 81 - 90 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