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
  • congenital myopathy 5
  • congenital myopathy
  • congenital nervous system abnormality
  • congenital nonspherocytic hemolytic anemia
  • congenital stationary night blindness 1A
  • congenital stationary night blindness autosomal dominant 2
  • congenital stationary night blindness
  • congenital stromal corneal dystrophy
  • congenital structural myopathy
  • congenital sucrase-isomaltase deficiency
Displaying entries 761 - 770 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