GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB), DisGeNET, and Alliance of Genome Resources is integrated into one list.

Database Last Updated
Alliance of Genome Resources February 28, 2024
DisGeNET February 14, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Disease ID Disease Name Gene Symbol Gene ID ▼
DOID:12177
  • common variable immunodeficiency
DOID:5709
  • mixed-type liposarcoma
DOID:0112072
  • nuclear type mitochondrial complex I deficiency 20
DOID:0080155
  • very long chain acyl-CoA dehydrogenase deficiency
DOID:0060230
  • basal ganglia calcification
DOID:13366
  • Stiff-Person syndrome
DOID:0090031
  • D-bifunctional protein deficiency
DOID:0050857
  • Perrault syndrome
DOID:0112248
  • 17-beta hydroxysteroid dehydrogenase 3 deficiency
DOID:4367
  • apparent mineralocorticoid excess syndrome
Displaying entries 531 - 540 of 1885 in total
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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

  • © GlyCosmos Portal v3.5.0
  • Last updated: March 25, 2024