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
Guidelines
MIRAGE
Alliance of Genome Resources

Alliance of Genome Resources is a gene dataset, which contains curated genome information essential for the understanding of the genetics and genomic basis of human biology, health and disease. All data is retrieved from six major model organism databases and the Gene Ontology including FlyBase, Mouse Genome Database (MGI), Rat Genome Database (RGD), Saccharomyces Genome Database (SGD), WormBase, Zebrafish Information Network (ZFIN), and the GO Consortium. In GlyCosmos, only glycan-related disease information has been extracted from Alliance of Genome Resources.

Source Last Updated
Alliance of Genome Resources January 28, 2025
Displaying entries 5976 - 6000 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID ▲ Species Gene ID Gene Symbol FlyGlycoDB Evidence References
DOID:3525 middle cerebral artery infarction HGNC:3530 Homo sapiens (human) 2161 F12 direct assay evidence used in manual assertion
  • PMID:16533887
DOID:5844 myocardial infarction HGNC:3530 Homo sapiens (human) 2161 F12 inference by association of genotype from phenotype used in manual assertion
  • PMID:16411408
DOID:2349 arteriosclerosis HGNC:3531 Homo sapiens (human) 2162 F13A1 inference by association of genotype from phenotype used in manual assertion
  • PMID:11941274
DOID:9286 priapism HGNC:3531 Homo sapiens (human) 2162 F13A1 inference by association of genotype from phenotype used in manual assertion
  • PMID:17408468
DOID:11247 disseminated intravascular coagulation HGNC:3531 Homo sapiens (human) 2162 F13A1 direct assay evidence used in manual assertion
  • PMID:16642548
DOID:5844 myocardial infarction HGNC:3531 Homo sapiens (human) 2162 F13A1 inference by association of genotype from phenotype used in manual assertion
  • PMID:12480694
  • RGD:7240710
DOID:0111907 thrombophilia due to thrombin defect HGNC:3531 Homo sapiens (human) 2162 F13A1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:2211 factor XIII deficiency HGNC:3531 Homo sapiens (human) 2162 F13A1 inference by association of genotype from phenotype used in manual assertion
  • PMID:19438481
  • PMID:19937244
  • PMID:20179087
  • PMID:21512576
  • PMID:23508224
DOID:9477 pulmonary embolism HGNC:3531 Homo sapiens (human) 2162 F13A1 direct assay evidence used in manual assertion
  • PMID:12958612
DOID:12134 factor VIII deficiency HGNC:3535 Homo sapiens (human) 2147 F2 direct assay evidence used in manual assertion
  • PMID:26635073
DOID:13001 carotid stenosis HGNC:3535 Homo sapiens (human) 2147 F2 inference by association of genotype from phenotype used in manual assertion
  • PMID:15748240
DOID:8536 herpes zoster HGNC:3535 Homo sapiens (human) 2147 F2 mutant phenotype evidence used in manual assertion
  • PMID:11449671
DOID:10159 osteonecrosis HGNC:3535 Homo sapiens (human) 2147 F2 inference by association of genotype from phenotype used in manual assertion
  • PMID:16968732
DOID:9074 systemic lupus erythematosus HGNC:3535 Homo sapiens (human) 2147 F2 direct assay evidence used in manual assertion
  • PMID:20807656
DOID:9074 systemic lupus erythematosus HGNC:3535 Homo sapiens (human) 2147 F2 inference by association of genotype from phenotype used in manual assertion
  • PMID:21239755
DOID:0111907 thrombophilia due to thrombin defect HGNC:3535 Homo sapiens (human) 2147 F2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:12259 hemophilia B HGNC:3535 Homo sapiens (human) 2147 F2 direct assay evidence used in manual assertion
  • PMID:26635073
DOID:5614 eye disease HGNC:3535 Homo sapiens (human) 2147 F2 inference by association of genotype from phenotype used in manual assertion
  • PMID:15077257
DOID:9477 pulmonary embolism HGNC:3535 Homo sapiens (human) 2147 F2 inference by association of genotype from phenotype used in manual assertion
  • PMID:25316662
DOID:12205 dengue disease HGNC:3535 Homo sapiens (human) 2147 F2 direct assay evidence used in manual assertion
  • PMID:22138554
DOID:2048 autoimmune hepatitis HGNC:3535 Homo sapiens (human) 2147 F2 direct assay evidence used in manual assertion
  • PMID:20821236
DOID:5844 myocardial infarction HGNC:3535 Homo sapiens (human) 2147 F2 inference by association of genotype from phenotype used in manual assertion
  • PMID:12480694
DOID:2235 prothrombin deficiency HGNC:3535 Homo sapiens (human) 2147 F2 inference by association of genotype from phenotype used in manual assertion
  • PMID:1349838
  • PMID:14629473
  • PMID:8839854
DOID:2921 glomerulonephritis HGNC:3535 Homo sapiens (human) 2147 F2 direct assay evidence used in manual assertion
  • PMID:17519558
DOID:1727 retinal vein occlusion HGNC:3535 Homo sapiens (human) 2147 F2 direct assay evidence used in manual assertion
  • PMID:22800650
Download data in CSV format Download data in TSV format Download data in JSON format
About Release Notes Help Feedback
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 v4.2.1

Last updated: April 7, 2025