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 October 28, 2022
DisGeNET June 29,2021
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Disease ID ▲ Disease Name Gene Symbol Gene ID
  • dilated cardiomyopathy 1X
  • X-linked dilated cardiomyopathy
  • autosomal recessive nonsyndromic deafness 21
  • autosomal recessive nonsyndromic deafness 22
  • autosomal dominant nonsyndromic deafness 12
  • primary ciliary dyskinesia 28
  • megaconial type congenital muscular dystrophy
  • muscular dystrophy-dystroglycanopathy type B5
  • muscular dystrophy-dystroglycanopathy type B6
  • long QT syndrome 2
Displaying entries 511 - 520 of 1611 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