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
Disease Name Gene Symbol Disease Name Aliases Disease Type UniProt ID Disease IDs
MPDU1
  • CDG-If
  • Congenital disorder of glycosylation, type If
Congenital Disorders of Glycosylation (CDGs)
  • C535744
  • MONDO:0012211
FKRP
  • Congenital muscular dystrophy type 1C (CMD1C)
  • FKRP-CDG (cong. muscular dystrophy spectrum)
  • Muscular dystrophy, congenital, type 1C (MDC1C)
  • Muscular dystrophy-dystroglycanopathy (Congenital with or without mental retardation), type B, 5 (MDDGB5)
Congenital Disorders of Glycosylation (CDGs)
  • C564691
  • MONDO:0011688
TMEM15
  • CDG-Im
  • Congenital disorder of glycosylation, type Im
  • DK1 deficiency
  • DK1-CDG
  • Dolichol kinase deficiency
Congenital Disorders of Glycosylation (CDGs)
  • C563666
  • MONDO:0012556
GUSB
  • MPS VII
  • Sly syndrome
Lysosomal Storage Diseases (LSDs)
  • D016538
  • DOID:12803
  • MONDO:0009662
HEXA
  • GM2-Gangliosidosis, B variant
  • GM2-gangliosidosis, type I
  • Hexosaminidase A deficiency
Lysosomal Storage Diseases (LSDs)
  • D013661
  • DOID:3320
  • MONDO:0010100
PIGM
  • Autosomal recessive GPI anchor deficiency
  • Glycosylphosphatidylinositol deficiency
Congenital Disorders of Glycosylation (CDGs)
  • C537277
GNE
  • GNE-CDG (hereditary inclusion body myopathy)
  • Hereditary inclusion body myopathy type 2 (HIBM2)
  • Inclusion body myopathy 2, autosomal recessive (IBM2)
Congenital Disorders of Glycosylation (CDGs)
  • C538329
ARSA
Lysosomal Storage Diseases (LSDs)
  • D007966
  • DOID:10581
  • MONDO:0018868
SLC26A2
  • ACG1B
  • Achondrogenesis, Fraccaro type
Congenital Disorders of Glycosylation (CDGs)
  • C536016
ASAH1
  • Acid Ceramidase Deficiency
Lysosomal Storage Diseases (LSDs)
  • D055577
  • DOID:0050464
  • MONDO:0009218
Displaying entries 21 - 30 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