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 10776 - 10800 of 15957 in total
Disease ID ▼ Disease Name Gene Symbol Gene ID Organism Source
DOID:0081441
  • Nicolaides-Baraitser syndrome
  • Aliases:
    • Intellectual disability-sparse hair-brachydactyly syndrome
    • SPARSE HAIR-IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME
Mus musculus (house mouse)
DOID:0081440
  • Peroxisome biogenesis disorder 10B
Homo sapiens (human)
DOID:0081430
  • intellectual developmental disorder with autistic features and language delay, with or without seizures
  • Aliases:
    • IDDALDS
Homo sapiens (human)
DOID:0081430
  • intellectual developmental disorder with autistic features and language delay, with or without seizures
  • Aliases:
    • IDDALDS
Rattus norvegicus (Norway rat)
DOID:0081430
  • intellectual developmental disorder with autistic features and language delay, with or without seizures
  • Aliases:
    • IDDALDS
Mus musculus (house mouse)
DOID:0081427
  • autosomal recessive distal hereditary motor neuronopathy 8
  • Aliases:
    • SORDD
    • sorbitol dehydrogenase deficiency with peripheral neuropathy
Mus musculus (house mouse)
DOID:0081427
  • autosomal recessive distal hereditary motor neuronopathy 8
  • Aliases:
    • SORDD
    • sorbitol dehydrogenase deficiency with peripheral neuropathy
Rattus norvegicus (Norway rat)
DOID:0081427
  • autosomal recessive distal hereditary motor neuronopathy 8
  • Aliases:
    • SORDD
    • sorbitol dehydrogenase deficiency with peripheral neuropathy
Saccharomyces cerevisiae S288C
DOID:0081427
  • autosomal recessive distal hereditary motor neuronopathy 8
  • Aliases:
    • SORDD
    • sorbitol dehydrogenase deficiency with peripheral neuropathy
Homo sapiens (human)
DOID:0081426
  • autosomal recessive distal hereditary motor neuronopathy 7
Homo sapiens (human)
DOID:0081426
  • autosomal recessive distal hereditary motor neuronopathy 7
Mus musculus (house mouse)
DOID:0081426
  • autosomal recessive distal hereditary motor neuronopathy 7
Rattus norvegicus (Norway rat)
DOID:0081424
  • familial focal epilepsy with variable foci 4
Homo sapiens (human)
DOID:0081424
  • familial focal epilepsy with variable foci 4
Rattus norvegicus (Norway rat)
DOID:0081424
  • familial focal epilepsy with variable foci 4
Mus musculus (house mouse)
DOID:0081424
  • familial focal epilepsy with variable foci 4
Drosophila melanogaster (fruit fly)
DOID:0081423
  • familial focal epilepsy with variable foci 3
Saccharomyces cerevisiae S288C
DOID:0081423
  • familial focal epilepsy with variable foci 3
Mus musculus (house mouse)
DOID:0081423
  • familial focal epilepsy with variable foci 3
Homo sapiens (human)
DOID:0081421
  • familial focal epilepsy with variable foci 1
Mus musculus (house mouse)
DOID:0081421
  • familial focal epilepsy with variable foci 1
Saccharomyces cerevisiae S288C
DOID:0081421
  • familial focal epilepsy with variable foci 1
Homo sapiens (human)
DOID:0081419
  • childhood-onset dystonia with optic atrophy and basal ganglia abnormalities
  • Aliases:
    • DYSTONIA 29, CHILDHOOD-ONSET
    • DYTOABG
    • MECR-related neurologic disorder
    • MEPAN syndrome
    • Mitochondrial Enoyl CoA Reductase Protein-Associated Neurodegeneration
Homo sapiens (human)
DOID:0081401
  • autosomal dominant distal hereditary motor neuronopathy 13
Homo sapiens (human)
DOID:0081401
  • autosomal dominant distal hereditary motor neuronopathy 13
Rattus norvegicus (Norway rat)
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