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
  • hereditary spastic paraplegia 3A
  • hereditary sensory neuropathy type 1D
  • hereditary sensory neuropathy type 1F
  • mitochondrial complex V (ATP synthase) deficiency nuclear type 3
  • immunodeficiency 47
  • congenital disorder of glycosylation type II
  • syndromic X-linked intellectual disability
  • syndromic X-linked intellectual disability Hedera type
  • X-linked parkinsonism-spasticity syndrome
  • renal tubular acidosis
Displaying entries 451 - 460 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