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 ▼
GM2-gangliosidosis, AB variant
GM2A
  • GM2 activator deficiency
  • Tay-Sachs disease, AB variant
Lysosomal Storage Diseases (LSDs)
Alpha-mannosidosis
MAN2B1
  • Alpha-mannosidase B deficiency
Lysosomal Storage Diseases (LSDs)
Alpha-mannosidosis, type I (early-onset)
MAN2B1
Lysosomal Storage Diseases (LSDs)
Alpha-mannosidosis, type II (later-onset)
MAN2B1
Lysosomal Storage Diseases (LSDs)
Sialidosis
NEU1
  • Mucolipidosis I
  • Neuraminidase deficiency
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)
Sandhoff disease
HEXB
  • GM2-gangliosidosis, type II
Lysosomal Storage Diseases (LSDs)
Sandhoff disease, infantile form
HEXB
Lysosomal Storage Diseases (LSDs)
Sandhoff disease, juvenile form
HEXB
Lysosomal Storage Diseases (LSDs)
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