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
LIPA
  • Acid lipase deficiency
  • Lysosomal acid lipase deficiency
Lysosomal Storage Diseases (LSDs)
  • D015223
  • DOID:14497
  • MONDO:0019148
C1GALT1C1
  • Galactosyltransferase Deficiency
  • Tn syndrome (SOMATIC MUTATION)
Congenital Disorders of Glycosylation (CDGs)
  • C562719
  • MONDO:0010381
CHSY1
  • TPBS
Congenital Disorders of Glycosylation (CDGs)
  • C536958
  • MONDO:0011533
HEXA
  • Juvenile/Chronic/Adult-onset
Lysosomal Storage Diseases (LSDs)
  • D013661
  • DOID:3320
  • MONDO:0010100
HEXA
  • Acute infantile
Lysosomal Storage Diseases (LSDs)
  • D013661
  • DOID:3320
  • MONDO:0010100
HEXA
  • GM2-Gangliosidosis, B variant
  • GM2-gangliosidosis, type I
  • Hexosaminidase A deficiency
Lysosomal Storage Diseases (LSDs)
  • D013661
  • DOID:3320
  • MONDO:0010100
TUSC3
  • Mental retardation, autosomal recessive 22
  • Mental retardation, autosomal recessive 7 (MRT7)
  • Oligosaccharyltransferase TUSC3 subunit defect
Congenital Disorders of Glycosylation (CDGs)
TMEM165
  • CDG-IIk
  • Congenital Disorder of Glycosylation, Type IIk
Congenital Disorders of Glycosylation (CDGs)
CHST3
  • Spondyloepiphyseal dysplasia, Omani type
Congenital Disorders of Glycosylation (CDGs)
  • C535789
PAPSS2
  • Brachyolmia 4 with mild epiphyseal and metaphyseal changes
  • SEMD, pakistani type
Congenital Disorders of Glycosylation (CDGs)
  • C567551
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