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
DOID:0110820
  • hereditary spastic paraplegia 75
DOID:0110839
  • Usher syndrome type 2C
DOID:0110852
  • rhizomelic chondrodysplasia punctata type 2
DOID:0110853
  • rhizomelic chondrodysplasia punctata type 3
DOID:0110858
  • polycystic kidney disease 1
DOID:0110859
  • polycystic kidney disease 2
DOID:0110860
  • polycystic kidney disease 3
DOID:0110861
  • autosomal recessive polycystic kidney disease
DOID:0110863
  • congenital stationary night blindness autosomal dominant 2
DOID:0110870
  • congenital stationary night blindness 1A
Displaying entries 681 - 690 of 1885 in total
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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

  • © GlyCosmos Portal v3.5.0
  • Last updated: March 25, 2024