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 June 29,2021
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Disease ID Disease Name Gene Symbol Gene ID ▲
  • optic atrophy 9
  • infantile cerebellar-retinal degeneration
  • pyridoxine-dependent epilepsy
  • lissencephaly 1
  • CHILD syndrome
  • Bloch-Sulzberger syndrome
  • CK syndrome
  • pyruvate carboxylase deficiency disease
  • propionic acidemia
  • Leber hereditary optic neuropathy with demyelinating disease of CNS
Displaying entries 1531 - 1540 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