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
Alpha-mannosidosis, type I (early-onset)
MAN2B1
Lysosomal Storage Diseases (LSDs)
Alpha-mannosidosis, type II (later-onset)
MAN2B1
Lysosomal Storage Diseases (LSDs)
Beta-mannosidosis
MANBA
  • Beta-mannosidase deficiency
Lysosomal Storage Diseases (LSDs)
Sialidosis
NEU1
  • Mucolipidosis I
  • Neuraminidase deficiency
Lysosomal Storage Diseases (LSDs)
Sialidosis type I
NEU1
  • Cherry-red spot myoclonus syndrome
  • Normosomatic sialidosis
Lysosomal Storage Diseases (LSDs)
Sialidosis type II
NEU1
  • Dysmorphic sialidosis
  • Neuraminidase 1 deficiency
Lysosomal Storage Diseases (LSDs)
Sialidosis type II, congenital form
NEU1
Lysosomal Storage Diseases (LSDs)
Sialidosis type II, infantile form
NEU1
Lysosomal Storage Diseases (LSDs)
Sialidosis type II, juvenile form
NEU1
Lysosomal Storage Diseases (LSDs)
Schindler disease, type I
NAGA
  • infantile type
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