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)
Galactosialidosis
CTSA
  • Combined deficiency of sialidase AND beta galactosidase
Lysosomal Storage Diseases (LSDs)
Mucolipidosis II (alpha/beta)
GNPTAB
  • I-cell disease
  • ML-II
  • N-Acetylglucosamine-1-phosphotransferase deficiency
Lysosomal Storage Diseases (LSDs)
Mucolipidosis III (alpha/beta)
GNPTAB
  • ML-III
  • Pseudo-Hurler Polydystrophy
Lysosomal Storage Diseases (LSDs)
Hurler syndrome
IDUA
  • Gargoylism, Hurler syndrome
  • MPS1-H
  • Mucopolysaccharidosis type IH
  • Pfaundler-Hurler syndrome
Lysosomal Storage Diseases (LSDs)
Hurler-Scheie syndrome
IDUA
  • MPS1-HS
  • Mucopolysaccharidosis type IH/S
Lysosomal Storage Diseases (LSDs)
Scheie syndrome
IDUA
  • MPS1-S
  • Mucopolysaccharidosis type IS
  • Mucopolysaccharidosis type V
  • Scheie's syndrome
Lysosomal Storage Diseases (LSDs)
Mucopolysaccharidosis II
IDS
  • Hunter syndrome
  • MPS II
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)
Displaying entries 91 - 100 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