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
  • hereditary spastic paraplegia 42
  • Sandhoff disease
  • non-syndromic X-linked intellectual disability 21
  • eosinophilic esophagitis
  • hereditary spastic paraplegia 75
  • hereditary spastic paraplegia 46
  • pyruvate kinase deficiency of red cells
  • diaphyseal medullary stenosis with malignant fibrous histiocytoma
  • distal hereditary motor neuronopathy type 5A
  • obsolete distal hereditary motor neuronopathy type 5A
  • islet cell tumor
Displaying entries 1611 - 1620 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