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
  • Charcot-Marie-Tooth disease type 2B2
  • hyperphosphatasia with impaired intellectual development syndrome 2
  • perinatal necrotizing enterocolitis
  • MASA syndrome
  • Keipert syndrome
  • nemaline myopathy
  • neonatal abstinence syndrome
  • hyperinsulinism
  • Alzheimer's disease 8
  • autosomal dominant limb-girdle muscular dystrophy type 1H
Displaying entries 101 - 110 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