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 7976 - 8000 of 15957 in total
Disease ID ▼ Disease Name Gene Symbol Gene ID Organism Source
DOID:0111745
  • cerebellar ataxia type 43
  • Aliases:
    • SCA43
Drosophila melanogaster (fruit fly)
DOID:0111745
  • cerebellar ataxia type 43
  • Aliases:
    • SCA43
Caenorhabditis elegans
DOID:0111745
  • cerebellar ataxia type 43
  • Aliases:
    • SCA43
Mus musculus (house mouse)
DOID:0111744
  • cerebellar ataxia type 41
  • Aliases:
    • SCA41
Homo sapiens (human)
DOID:0111744
  • cerebellar ataxia type 41
  • Aliases:
    • SCA41
Mus musculus (house mouse)
DOID:0111743
  • cerebellar ataxia type 47
  • Aliases:
    • SCA47
Saccharomyces cerevisiae S288C
DOID:0111743
  • cerebellar ataxia type 47
  • Aliases:
    • SCA47
Homo sapiens (human)
DOID:0111743
  • cerebellar ataxia type 47
  • Aliases:
    • SCA47
Mus musculus (house mouse)
DOID:0111742
  • cerebellar ataxia type 42
  • Aliases:
    • SCA42
Homo sapiens (human)
DOID:0111742
  • cerebellar ataxia type 42
  • Aliases:
    • SCA42
Mus musculus (house mouse)
DOID:0111741
  • X-linked deafness 5
  • Aliases:
    • AUNX1
    • DFNX5
    • X-linked HSAN with deafness
    • X-linked auditory neuropathy 1 with peripheral sensory neuropathy
    • X-linked auditory neuropathy with peripheral sensory neuropathy type 1
Mus musculus (house mouse)
DOID:0111741
  • X-linked deafness 5
  • Aliases:
    • AUNX1
    • DFNX5
    • X-linked HSAN with deafness
    • X-linked auditory neuropathy 1 with peripheral sensory neuropathy
    • X-linked auditory neuropathy with peripheral sensory neuropathy type 1
Homo sapiens (human)
DOID:0111740
  • X-linked deafness 6
  • Aliases:
    • DFNX6
Drosophila melanogaster (fruit fly)
DOID:0111740
  • X-linked deafness 6
  • Aliases:
    • DFNX6
Caenorhabditis elegans
DOID:0111740
  • X-linked deafness 6
  • Aliases:
    • DFNX6
Homo sapiens (human)
DOID:0111739
  • X-linked deafness 1
  • Aliases:
    • DFN2
    • DFNX1
    • X-linked sensorineural congenital deafness 2
Homo sapiens (human)
DOID:0111739
  • X-linked deafness 1
  • Aliases:
    • DFN2
    • DFNX1
    • X-linked sensorineural congenital deafness 2
Mus musculus (house mouse)
DOID:0111738
  • X-linked deafness 7
  • Aliases:
    • DFNX7
    • X-linked external auditory canal atresia-dilated internal auditory canal-facial dysmorphism syndrome
Mus musculus (house mouse)
DOID:0111735
  • X-linked deafness 4
  • Aliases:
    • DFN6
    • DFNX4
    • X-linked progressive deafness 6
    • nonsyndromic sensorineural progressive deafness 6
Homo sapiens (human)
DOID:0111732
  • Eiken syndrome
  • Aliases:
    • Eiken skeletal dysplasia
    • bone modeling defect of hands and feet
Caenorhabditis elegans
DOID:0111732
  • Eiken syndrome
  • Aliases:
    • Eiken skeletal dysplasia
    • bone modeling defect of hands and feet
Rattus norvegicus (Norway rat)
DOID:0111732
  • Eiken syndrome
  • Aliases:
    • Eiken skeletal dysplasia
    • bone modeling defect of hands and feet
Mus musculus (house mouse)
DOID:0111732
  • Eiken syndrome
  • Aliases:
    • Eiken skeletal dysplasia
    • bone modeling defect of hands and feet
Homo sapiens (human)
DOID:0111731
  • familial episodic pain syndrome 3
  • Aliases:
    • FEPS3
Mus musculus (house mouse)
DOID:0111731
  • familial episodic pain syndrome 3
  • Aliases:
    • FEPS3
Homo sapiens (human)
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