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
SLC35A1-CDG
SLC35A1
  • CDG-IIf
  • Congenital disorder of glycosylation, type IIf
Congenital Disorders of Glycosylation (CDGs)
SLC35C1-CDG
SLC35C1
  • CDG-IIc
  • Congenital disorder of glycosylation, type IIc
  • Leukocyte adhesion deficiency, type 2
  • Rambam Hasharon syndrome
Congenital Disorders of Glycosylation (CDGs)
SLC35D1-CDG
SLC35D1
  • Chondrodysplasia, lethal neonatal, with snail-like pelvis
  • Schneckenbecken dysplasia
Congenital Disorders of Glycosylation (CDGs)
SRD5A3-CDG
SRD5A3
  • CDG-Iq
  • Congenital Disorder of Glycosylation, Type Iq
  • Ocular colobomas, ichthyosis, brain malformations and endocrine abnormalities
Congenital Disorders of Glycosylation (CDGs)
ST3GAL5-CDG
SIAT9
  • Amish infantile epilepsy syndrome
  • Epilepsy syndrome, infantile-onset symptomatic
  • GM3 Synthase deficiency
Congenital Disorders of Glycosylation (CDGs)
Sandhoff disease
HEXB
  • GM2-gangliosidosis, type II
Lysosomal Storage Diseases (LSDs)
Sandhoff disease, adult form
HEXB
Lysosomal Storage Diseases (LSDs)
Sandhoff disease, infantile form
HEXB
Lysosomal Storage Diseases (LSDs)
Sandhoff disease, juvenile form
HEXB
Lysosomal Storage Diseases (LSDs)
Sanfilippo syndrome A
SGSH
  • MPS IIIA
  • Mucopolysaccharidosis type IIIA
Lysosomal Storage Diseases (LSDs)
Displaying entries 121 - 130 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