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 12651 - 12675 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism Source
DOID:0080986
  • Ehlers-Danlos syndrome periodontal type 1
Mus musculus (house mouse)
DOID:3651
  • pyruvate carboxylase deficiency disease
  • Aliases:
    • deficiency of pyruvic carboxylase
Homo sapiens (human)
DOID:0111391
  • mucopolysaccharidosis IVA
  • Aliases:
    • GALNS deficiency
    • MPS IVA
    • MPS4A
    • Morquio A disease
    • Morquio syndrome A
Mus musculus (house mouse)
DOID:0110877
  • holoprosencephaly 11
  • Aliases:
    • HPE11
Homo sapiens (human)
DOID:0110877
  • holoprosencephaly 11
  • Aliases:
    • HPE11
Rattus norvegicus (Norway rat)
DOID:0110371
  • retinitis pigmentosa 56
  • Aliases:
    • RP56
Homo sapiens (human)
DOID:14701
  • propionic acidemia
  • Aliases:
    • GLYCINEMIA, KETOTIC
    • KETOTIC HYPERGLYCINEMIA
    • ketotic II glycinemia
    • ketotic glycinemia
    • propionic aciduria
    • propionyl-CoA carboxylase deficiency
Homo sapiens (human)
DOID:0080036
  • SOST-related sclerosing bone dysplasia
  • Aliases:
    • van Buchem disease
Homo sapiens (human)
DOID:0080807
  • autosomal dominant craniodiaphyseal dysplasia
Homo sapiens (human)
DOID:0060251
  • sclerosteosis
Homo sapiens (human)
DOID:0060756
  • sclerosteosis 1
  • Aliases:
    • SOST1
Homo sapiens (human)
DOID:0050797
  • peroxisomal acyl-CoA oxidase deficiency
  • Aliases:
    • Peroxisomal acyl-coenzyme A oxidase
Homo sapiens (human)
DOID:0070516
  • Mitchell syndrome
Homo sapiens (human)
DOID:3204
  • schwannomatosis
  • Aliases:
    • SWN
    • neurilemmomatosis
    • neurinomatosis
Homo sapiens (human)
DOID:0070243
  • primary coenzyme Q10 deficiency 6
  • Aliases:
    • COQ10D6
    • coenzyme Q10 deficiency, primary, 6
    • familial steroid-resistant nephrotic syndrome with sensorineural deafness
Homo sapiens (human)
DOID:0080517
  • Meier-Gorlin syndrome 6
Homo sapiens (human)
DOID:0111186
  • myopathy, lactic acidosis, and sideroblastic anemia 2
  • Aliases:
    • MLASA2
Homo sapiens (human)
DOID:0060754
  • familial temporal lobe epilepsy 8
  • Aliases:
    • ETL8
Homo sapiens (human)
DOID:1188
  • mononeuropathy
Homo sapiens (human)
DOID:0080209
  • sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay
  • Aliases:
    • SIFD
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:0111756
  • Leber hereditary optic neuropathy with demyelinating disease of CNS
Homo sapiens (human)
DOID:0081385
  • ataxia-telangiectasia-like disorder-2
  • Aliases:
    • PCNA-related progressive neurodegenerative photosensitivity syndrome
Homo sapiens (human)
DOID:0080232
  • autosomal dominant intellectual developmental disorder 51
  • Aliases:
    • autosomal dominant mental retardation 51
Homo sapiens (human)
DOID:0070098
  • oculocutaneous albinism type IV
  • Aliases:
    • OCA4
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