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
  • oligospermia
  • congenital disorder of glycosylation type IIa
  • dominant optic atrophy plus syndrome
  • mitochondrial DNA depletion syndrome 14
  • Behr syndrome
  • methylmalonic acidemia cblA type
  • methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency
  • Charcot-Marie-Tooth disease axonal type 2Z
  • congenital disorder of glycosylation Ib
  • Noonan syndrome 11
Displaying entries 1411 - 1420 of 1885 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