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
GCS1-CDG
GCS1
  • CDG-IIb
  • Congenital disorder of glycosylation, type IIb
  • MOGS-CDG
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)
B4GALT1-CDG
B4GALT1
  • CDG-IId
  • Congenital disorder of glycosylation, type IId
Congenital Disorders of Glycosylation (CDGs)
COG7-CDG
COG7
  • CDG-IIe
  • Congenital disorder of glycosylation, type IIe
Congenital Disorders of Glycosylation (CDGs)
SLC35A1-CDG
SLC35A1
  • CDG-IIf
  • Congenital disorder of glycosylation, type IIf
Congenital Disorders of Glycosylation (CDGs)
COG1-CDG
COG1
  • CDG-IIg
  • CDGII/COG1 Cerebrocostomandibular-like syndrome
  • COG1 deficiency
  • Congenital disorder of glycosylation, type IIg
Congenital Disorders of Glycosylation (CDGs)
COG8-CDG
COG8
  • CDG-IIh
  • COG8 deficiency
  • Congenital disorder of glycosylation, type IIh
Congenital Disorders of Glycosylation (CDGs)
COG5-CDG
COG5
  • CDG-IIi
  • Congenital disorder of glycosylation, type IIi
Congenital Disorders of Glycosylation (CDGs)
COG4-CDG
COG4
  • CDG-IIj
  • Congenital disorder of glycosylation, type IIj
Congenital Disorders of Glycosylation (CDGs)
TUSC3-CDG
TUSC3
  • Mental retardation, autosomal recessive 22
  • Mental retardation, autosomal recessive 7 (MRT7)
  • Oligosaccharyltransferase TUSC3 subunit defect
Congenital Disorders of Glycosylation (CDGs)
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