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 7926 - 7950 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source ▼
DOID:0111876
  • linear skin defects with multiple congenital anomalies 3
  • Aliases:
    • LSDMCA3
    • linear skin defects with cardiomyopathy and other congenital anomalies
Rattus norvegicus (Norway rat)
DOID:0111872
  • nonphotosensitive trichothiodystrophy 6
  • Aliases:
    • TTD6
Homo sapiens (human)
DOID:0111870
  • nonphotosensitive trichothiodystrophy 7
  • Aliases:
    • TTD7
Mus musculus (house mouse)
DOID:0111870
  • nonphotosensitive trichothiodystrophy 7
  • Aliases:
    • TTD7
Homo sapiens (human)
DOID:0111867
  • nonphotosensitive trichothiodystrophy
Homo sapiens (human)
DOID:0111867
  • nonphotosensitive trichothiodystrophy
Mus musculus (house mouse)
DOID:0111866
  • trichothiodystrophy
  • Aliases:
    • TTD
Homo sapiens (human)
DOID:0111866
  • trichothiodystrophy
  • Aliases:
    • TTD
Mus musculus (house mouse)
DOID:0111865
  • MEND syndrome
  • Aliases:
    • male EBP disorder with neurological defects
Mus musculus (house mouse)
DOID:0111865
  • MEND syndrome
  • Aliases:
    • male EBP disorder with neurological defects
Homo sapiens (human)
DOID:0111864
  • autosomal recessive congenital bilateral absence of vas deferens
Rattus norvegicus (Norway rat)
DOID:0111864
  • autosomal recessive congenital bilateral absence of vas deferens
Homo sapiens (human)
DOID:0111864
  • autosomal recessive congenital bilateral absence of vas deferens
Saccharomyces cerevisiae S288C
DOID:0111864
  • autosomal recessive congenital bilateral absence of vas deferens
Danio rerio (zebrafish)
DOID:0111864
  • autosomal recessive congenital bilateral absence of vas deferens
Mus musculus (house mouse)
DOID:0111863
  • X-linked congenital bilateral absence of vas deferens
  • Aliases:
    • CBAVDX
Rattus norvegicus (Norway rat)
DOID:0111863
  • X-linked congenital bilateral absence of vas deferens
  • Aliases:
    • CBAVDX
Homo sapiens (human)
DOID:0111863
  • X-linked congenital bilateral absence of vas deferens
  • Aliases:
    • CBAVDX
Mus musculus (house mouse)
DOID:0111862
  • congenital bilateral absence of vas deferens
  • Aliases:
    • CAVD
    • CBAVD
    • congenital bilateral agenesis of vas deferens
    • congenital bilateral aplasia of vas deferens
Mus musculus (house mouse)
DOID:0111862
  • congenital bilateral absence of vas deferens
  • Aliases:
    • CAVD
    • CBAVD
    • congenital bilateral agenesis of vas deferens
    • congenital bilateral aplasia of vas deferens
Homo sapiens (human)
DOID:0111862
  • congenital bilateral absence of vas deferens
  • Aliases:
    • CAVD
    • CBAVD
    • congenital bilateral agenesis of vas deferens
    • congenital bilateral aplasia of vas deferens
Saccharomyces cerevisiae S288C
DOID:0111862
  • congenital bilateral absence of vas deferens
  • Aliases:
    • CAVD
    • CBAVD
    • congenital bilateral agenesis of vas deferens
    • congenital bilateral aplasia of vas deferens
Danio rerio (zebrafish)
DOID:0111862
  • congenital bilateral absence of vas deferens
  • Aliases:
    • CAVD
    • CBAVD
    • congenital bilateral agenesis of vas deferens
    • congenital bilateral aplasia of vas deferens
Rattus norvegicus (Norway rat)
DOID:0111861
  • Meester-Loeys syndrome
  • Aliases:
    • MRLS
Rattus norvegicus (Norway rat)
DOID:0111861
  • Meester-Loeys syndrome
  • Aliases:
    • MRLS
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