Table Filtering
Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
LM-GlycoRepo
Repository for lectin-assisted multimodality data
Resources Genes Glycoproteins Lectins Glycolipids Glycans Pathways Diseases Organisms
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Other Information
Release Statistics Download
Tools
SugarDrawer GlycanBuilder Glycan Converters GlycoMaple GlycomeAtlas LM-GlycomeAtlas GALAXY MCAW GlycoSim GRable
Search Tools
Cross Search Glycan Search Publication Search Programmatic Access
Standards Ontologies Notations
GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB) and Alliance of Genome Resources is integrated into one list.

Source Last Updated
Alliance of Genome Resources October 9, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 13776 - 13800 of 15957 in total
Disease ID Disease Name ▼ Gene Symbol Gene ID Organism Source
DOID:0110827
  • Usher syndrome type 2
  • Aliases:
    • USH2
Mus musculus (house mouse)
DOID:0110832
  • Usher syndrome type 1F
  • Aliases:
    • USH1F
    • Usher syndrome type IF
Homo sapiens (human)
DOID:0110832
  • Usher syndrome type 1F
  • Aliases:
    • USH1F
    • Usher syndrome type IF
Drosophila melanogaster (fruit fly)
DOID:0110832
  • Usher syndrome type 1F
  • Aliases:
    • USH1F
    • Usher syndrome type IF
Mus musculus (house mouse)
DOID:0110831
  • Usher syndrome type 1D
  • Aliases:
    • USH1D
    • Usher syndrome type ID
Drosophila melanogaster (fruit fly)
DOID:0110831
  • Usher syndrome type 1D
  • Aliases:
    • USH1D
    • Usher syndrome type ID
Mus musculus (house mouse)
DOID:0110831
  • Usher syndrome type 1D
  • Aliases:
    • USH1D
    • Usher syndrome type ID
Homo sapiens (human)
DOID:0110831
  • Usher syndrome type 1D
  • Aliases:
    • USH1D
    • Usher syndrome type ID
Rattus norvegicus (Norway rat)
DOID:0110826
  • Usher syndrome type 1
  • Aliases:
    • US1
    • USH1
Homo sapiens (human)
DOID:0112148
  • Uruguay faciocardiomusculoskeletal syndrome
  • Aliases:
    • FCMSU
Homo sapiens (human)
DOID:3535
  • Unverricht-Lundborg syndrome
  • Aliases:
    • Unverricht - Lundborg disease
    • Unverricht's disease
    • Unverricht-Lundborg disease
Homo sapiens (human)
DOID:0050558
  • Ullrich congenital muscular dystrophy
  • Aliases:
    • ULLRICH DISEASE
    • Ullrich scleroatonic muscular dystrophy
Homo sapiens (human)
DOID:0050558
  • Ullrich congenital muscular dystrophy
  • Aliases:
    • ULLRICH DISEASE
    • Ullrich scleroatonic muscular dystrophy
Mus musculus (house mouse)
DOID:0050558
  • Ullrich congenital muscular dystrophy
  • Aliases:
    • ULLRICH DISEASE
    • Ullrich scleroatonic muscular dystrophy
Caenorhabditis elegans
DOID:0060240
  • UV-sensitive syndrome
Homo sapiens (human)
DOID:0060240
  • UV-sensitive syndrome
Caenorhabditis elegans
DOID:3491
  • Turner syndrome
  • Aliases:
    • Bonnevie-Ullrich syndrome
    • Gonadal dysgenesis - Turner
    • Karyotype 45, X
    • Monosomy X
    • XO syndrome
    • monosomy X syndrome
Rattus norvegicus (Norway rat)
DOID:3491
  • Turner syndrome
  • Aliases:
    • Bonnevie-Ullrich syndrome
    • Gonadal dysgenesis - Turner
    • Karyotype 45, X
    • Monosomy X
    • XO syndrome
    • monosomy X syndrome
Mus musculus (house mouse)
DOID:3491
  • Turner syndrome
  • Aliases:
    • Bonnevie-Ullrich syndrome
    • Gonadal dysgenesis - Turner
    • Karyotype 45, X
    • Monosomy X
    • XO syndrome
    • monosomy X syndrome
Homo sapiens (human)
DOID:0050886
  • Troyer syndrome
  • Aliases:
    • SPG20
    • autosomal recessive spastic paraplegia 20
    • autosomal recessive spastic paraplegia Troyer type
    • autosomal recessive spastic paraplegia type 20
    • childhood-onset spastic paraparesis with distal muscle wasting
    • hereditary spastic paraplegia 20
    • spastic paraplegia 20
    • spastic paraplegia type 20
Homo sapiens (human)
DOID:0050886
  • Troyer syndrome
  • Aliases:
    • SPG20
    • autosomal recessive spastic paraplegia 20
    • autosomal recessive spastic paraplegia Troyer type
    • autosomal recessive spastic paraplegia type 20
    • childhood-onset spastic paraparesis with distal muscle wasting
    • hereditary spastic paraplegia 20
    • spastic paraplegia 20
    • spastic paraplegia type 20
Mus musculus (house mouse)
DOID:2908
  • Treacher Collins syndrome
  • Aliases:
    • Franceschetti syndrome
    • mandibulofacial dysostosis
Mus musculus (house mouse)
DOID:2908
  • Treacher Collins syndrome
  • Aliases:
    • Franceschetti syndrome
    • mandibulofacial dysostosis
Homo sapiens (human)
DOID:0080792
  • Treacher Collins syndrome 4
Homo sapiens (human)
DOID:0080789
  • Treacher Collins syndrome 1
Mus musculus (house mouse)
Download data in CSV format Download data in TSV format Download data in JSON format
About Release Notes Help Feedback

Click here to visit the beta site.

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

Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International

GlyCosmos Portal v4.1.0

Last updated: December 9, 2024