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 6901 - 6925 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:0080015
  • physical disorder
  • Aliases:
    • congenital disorder
Caenorhabditis elegans
DOID:14176
  • selective IgG deficiency disease
  • Aliases:
    • Immunoglobin G subclass deficiency
    • Selective IgG Immunodeficiency
    • Selective Immunoglobulin G Subclass deficiency
    • Selective deficiency of IgG
    • Selective immunoglobulin G deficiency
Rattus norvegicus (Norway rat)
DOID:0111973
  • immunodeficiency 17
  • Aliases:
    • CD3-gamma deficiency
    • IMD17
    • SCID-like immunodeficiency, T cell-partial, B cell-positive, NK cell-positive
    • immunodeficiency 17, CD3 gamma deficient
Homo sapiens (human)
DOID:0080493
  • ovarian dysgenesis 1
Mus musculus (house mouse)
DOID:0050563
  • nonsyndromic deafness
  • Aliases:
    • nonsyndromic hearing loss
    • nonsyndromic hereditary hearing loss
Drosophila melanogaster (fruit fly)
DOID:0080679
  • neuronal intestinal dysplasia type A
Homo sapiens (human)
DOID:0080521
  • lung non-squamous non-small cell carcinoma
  • Aliases:
    • non- squamous NSCLC
Homo sapiens (human)
DOID:12297
  • Vogt-Koyanagi-Harada disease
  • Aliases:
    • Harada's disease
    • Vogt-Koyanagi syndrome
    • uveomeningoencephalitic syndrome
Rattus norvegicus (Norway rat)
DOID:0050782
  • Zollinger-Ellison syndrome
Mus musculus (house mouse)
DOID:0110721
  • neuronal ceroid lipofuscinosis 1
  • Aliases:
    • CLN1
    • neuronal ceroid lipofuscinosis 1 variable age of onset
Homo sapiens (human)
DOID:0050588
  • muscular dystrophy-dystroglycanopathy type B1
  • Aliases:
    • CMD due to dystroglycanopathy
    • Muscular dystrophy-dystroglycanopathy congenital with impaired intellectual development B1
Xenopus tropicalis (tropical clawed frog)
DOID:0110814
  • hereditary spastic paraplegia 63
  • Aliases:
    • SPG63
    • autosomal recessive spastic paraplegia 63
    • spastic paraplegia 63
Homo sapiens (human)
DOID:1837
  • diabetic ketoacidosis
  • Aliases:
    • DIABETES MELLITUS, KETOSIS-PRONE
    • ketosis-prone diabetes mellitus
Homo sapiens (human)
DOID:0050737
  • autosomal recessive disease
Mus musculus (house mouse)
DOID:5602
  • T-cell adult acute lymphocytic leukemia
  • Aliases:
    • ATLL
    • Acute Adult T-cell Leukemia-Lymphoma
    • adult Precursor T Lymphoblastic Leukemia
Mus musculus (house mouse)
DOID:0080575
  • Larsen-like syndrome B3GAT3 type
  • Aliases:
    • Larsen-like syndrome, B3GAT3 type
    • multiple joint dislocations-short stature-craniofacial dysmorphism-congenital heart defects syndrome
Xenopus tropicalis (tropical clawed frog)
DOID:0070347
  • encephalopathy due to defective mitochondrial and peroxisomal fission 1
Homo sapiens (human)
DOID:0060387
  • chondrodysplasia Blomstrand type
  • Aliases:
    • Blomstrand lethal chondrodysplasia
Caenorhabditis elegans
DOID:1825
  • childhood absence epilepsy
  • Aliases:
    • petit mal seizure
    • pyknolepsy
Saccharomyces cerevisiae S288C
DOID:2219
  • Glanzmann's thrombasthenia
  • Aliases:
    • BDPLT2
    • Glanzmann thrombasthenia
    • Glycoprotein IIb/IIIa defect
    • Thrombocytasthenia
    • deficiency of GP IIb-IIIa complex
    • deficiency of glycoprotein complex IIb-IIIa
    • deficiency of platelet fibrinogen receptor
    • platelet glycoprotein IIb-IIIa deficiency
    • platelet-type bleeding disorder 2
    • thrombasthenia of Glanzmann and Naegeli
Homo sapiens (human)
DOID:14447
  • gonadal dysgenesis
  • Aliases:
    • Gonadal dysgenesis syndrome
Homo sapiens (human)
DOID:3209
  • junctional epidermolysis bullosa
  • Aliases:
    • congenital junctional epidermolysis bullosa
Caenorhabditis elegans
DOID:0050667
  • alcohol-related neurodevelopmental disorder
  • Aliases:
    • ARND
    • static encephalopathy
Drosophila melanogaster (fruit fly)
DOID:0111905
  • autosomal recessive thrombophilia due to protein S deficiency
  • Aliases:
    • THPH6
    • autosomal recessive thrombophilia due to congenital protein S deficiency
    • severe hereditary thrombophilia due to congenital protein S deficiency
Mus musculus (house mouse)
DOID:0110344
  • osteogenesis imperfecta type 5
  • Aliases:
    • OI5
    • osteogenesis imperfecta type V
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