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 7451 - 7475 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:0080236
  • autosomal dominant intellectual developmental disorder 45
  • Aliases:
    • autosomal dominant mental retardation 45
Mus musculus (house mouse)
DOID:0112277
  • immunodeficiency 79
  • Aliases:
    • IMD79
Rattus norvegicus (Norway rat)
DOID:0111678
  • hereditary folate malabsorption
  • Aliases:
    • congenital defect of folate absorption
    • congenital folate malabsorption
Homo sapiens (human)
DOID:0111370
  • apolipoprotein C-III deficiency
  • Aliases:
    • HALP2
    • hyperalphalipoproteinemia 2
Mus musculus (house mouse)
DOID:0070202
  • familial partial lipodystrophy type 2
  • Aliases:
    • FPLD2
    • familial lipodystrophy of limbs and lower trunk
    • familial partial lipodystrophy Dunnigan type
    • reverse partial lipodystrophy
Homo sapiens (human)
DOID:0070235
  • Loeys-Dietz syndrome 1
  • Aliases:
    • AAT5
    • Furlong syndrome
    • LDS1
    • familial throacic aortic aneurysm 5
Rattus norvegicus (Norway rat)
DOID:8618
  • oral cavity cancer
  • Aliases:
    • malignant neoplasm of floor of mouth
Homo sapiens (human)
DOID:0110661
  • congenital myasthenic syndrome 20
  • Aliases:
    • CMS20
    • congenital myasthenic syndrome 20 presynaptic
Rattus norvegicus (Norway rat)
DOID:106
  • pleural tuberculosis
  • Aliases:
    • Pearly disease
    • Tuberculosis of pleura
    • Tuberculous pleurisy
    • Tuberculous pleuritis
    • tuberculous pleurisy in primary progressive tuberculosis
Danio rerio (zebrafish)
DOID:5041
  • esophageal cancer
  • Aliases:
    • Ca lower third oesophagus
    • Ca middle third oesophagus
    • esophagus cancer
    • malignant neoplasm of distal third of esophagus
    • malignant neoplasm of lower third of oesophagus
    • malignant neoplasm of middle third of oesophagus
    • malignant neoplasm of proximal third of esophagus
    • malignant neoplasm of upper third esophagus
    • malignant tumor of Distal Third of esophagus
    • malignant tumor of Proximal Third of esophagus
    • malignant tumor of abdominal esophagus
    • malignant tumor of the middle Third of the esophagus
Mus musculus (house mouse)
DOID:0060393
  • chromosome 15q11.2 deletion syndrome
  • Aliases:
    • 15q11.2 microdeletion syndrome
Homo sapiens (human)
DOID:0080325
  • tuberous sclerosis 2
Mus musculus (house mouse)
DOID:0080339
  • familial erythrocytosis 4
  • Aliases:
    • ECYT4
Homo sapiens (human)
DOID:7147
  • ankylosing spondylitis
  • Aliases:
    • Bekhterev syndrome
    • Bekhterev's disease
    • Marie-Strumpell disease
Homo sapiens (human)
DOID:0080652
  • calcium oxalate nephrolithiasis
Rattus norvegicus (Norway rat)
DOID:0110704
  • hypotrichosis 7
  • Aliases:
    • Hypt7
    • Lah2
    • hypotrichosis, localized, autosomal recessive 2
    • total Mari type hypotrichosis,
Rattus norvegicus (Norway rat)
DOID:12308
  • Dubin-Johnson syndrome
  • Aliases:
    • Dubin Johnson syndrome
    • chronic idiopathic jaundice
Rattus norvegicus (Norway rat)
DOID:4440
  • seminoma
  • Aliases:
    • Seminoma, Pure
Homo sapiens (human)
DOID:13413
  • hepatic encephalopathy
  • Aliases:
    • Portal-systemic encephalopathy
Mus musculus (house mouse)
DOID:0070072
  • autosomal dominant intellectual developmental disorder 42
  • Aliases:
    • MRD42
    • autosomal dominant mental retardation 42
    • autosomal dominant non-syndromic intellectual disability 42
Homo sapiens (human)
DOID:0001816
  • angiosarcoma
  • Aliases:
    • hemangiosarcoma
Caenorhabditis elegans
DOID:2861
  • congenital nonspherocytic hemolytic anemia
  • Aliases:
    • HNSHA
    • congenital nonspherocytic hemolytic anaemia
    • hereditary nonspherocytic hemolytic anaemia
    • hereditary nonspherocytic hemolytic anemia
Caenorhabditis elegans
DOID:0080162
  • lupus nephritis
Mus musculus (house mouse)
DOID:0060684
  • autosomal dominant nocturnal frontal lobe epilepsy 3
  • Aliases:
    • ENFL3
    • nocturnal frontal lobe epilepsy 3
Drosophila melanogaster (fruit fly)
DOID:0111108
  • maturity-onset diabetes of the young type 10
  • Aliases:
    • MODY10
Danio rerio (zebrafish)
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