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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 6051 - 6075 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence References
DOID:2841 asthma HGNC:6001 Homo sapiens (human) 3558 IL2 inference by association of genotype from phenotype used in manual assertion
  • PMID:16333313
DOID:8506 bullous pemphigoid HGNC:6001 Homo sapiens (human) 3558 IL2 direct assay evidence used in manual assertion
  • PMID:1973607
DOID:10652 Alzheimer's disease HGNC:6001 Homo sapiens (human) 3558 IL2 direct assay evidence used in manual assertion
  • PMID:8915041
DOID:0081267 graft-versus-host disease HGNC:6001 Homo sapiens (human) 3558 IL2 direct assay evidence used in manual assertion
  • PMID:8704686
DOID:4450 renal cell carcinoma HGNC:6001 Homo sapiens (human) 3558 IL2 direct assay evidence used in manual assertion
  • PMID:21812652
DOID:4483 rhinitis HGNC:6001 Homo sapiens (human) 3558 IL2 inference by association of genotype from phenotype used in manual assertion
  • PMID:16333313
DOID:612 primary immunodeficiency disease HGNC:6001 Homo sapiens (human) 3558 IL2 direct assay evidence used in manual assertion
  • PMID:3048654
DOID:3310 atopic dermatitis HGNC:6001 Homo sapiens (human) 3558 IL2 inference by association of genotype from phenotype used in manual assertion
  • PMID:16333313
DOID:3070 high grade glioma HGNC:6001 Homo sapiens (human) 3558 IL2 direct assay evidence used in manual assertion
  • PMID:12864971
DOID:0081267 graft-versus-host disease HGNC:6001 Homo sapiens (human) 3558 IL2 mutant phenotype evidence used in manual assertion
  • PMID:21734238
DOID:12704 ataxia telangiectasia HGNC:6001 Homo sapiens (human) 3558 IL2 direct assay evidence used in manual assertion
  • PMID:6432389
DOID:9182 pemphigus HGNC:6001 Homo sapiens (human) 3558 IL2 direct assay evidence used in manual assertion
  • PMID:6432916
DOID:0081120 Graves ophthalmopathy HGNC:6001 Homo sapiens (human) 3558 IL2 direct assay evidence used in manual assertion
  • PMID:2786308
DOID:11446 sciatic neuropathy HGNC:6000 Homo sapiens (human) 3557 IL1RN direct assay evidence used in manual assertion
  • PMID:12574433
DOID:9538 multiple myeloma HGNC:6000 Homo sapiens (human) 3557 IL1RN inference by association of genotype from phenotype used in manual assertion
  • PMID:17926179
DOID:9352 type 2 diabetes mellitus HGNC:6000 Homo sapiens (human) 3557 IL1RN inference by association of genotype from phenotype used in manual assertion
  • PMID:17069782
  • PMID:21205020
DOID:10459 common cold HGNC:6000 Homo sapiens (human) 3557 IL1RN direct assay evidence used in manual assertion
  • PMID:18279051
DOID:4371 Schnitzler syndrome HGNC:6000 Homo sapiens (human) 3557 IL1RN direct assay evidence used in manual assertion
  • PMID:16096327
DOID:12554 hemolytic-uremic syndrome HGNC:6000 Homo sapiens (human) 3557 IL1RN direct assay evidence used in manual assertion
  • PMID:12373296
DOID:7148 rheumatoid arthritis HGNC:6000 Homo sapiens (human) 3557 IL1RN direct assay evidence used in manual assertion
  • PMID:19447938
DOID:10325 silicosis HGNC:6000 Homo sapiens (human) 3557 IL1RN inference by association of genotype from phenotype used in manual assertion
  • PMID:11264025
DOID:824 periodontitis HGNC:6000 Homo sapiens (human) 3557 IL1RN inference by association of genotype from phenotype used in manual assertion
  • PMID:22795294
DOID:8924 autoimmune thrombocytopenic purpura HGNC:6000 Homo sapiens (human) 3557 IL1RN inference by association of genotype from phenotype used in manual assertion
  • PMID:20626741
DOID:986 alopecia areata HGNC:6000 Homo sapiens (human) 3557 IL1RN inference by association of genotype from phenotype used in manual assertion
  • PMID:8077705
DOID:12894 Sjogren's syndrome HGNC:6000 Homo sapiens (human) 3557 IL1RN inference by association of genotype from phenotype used in manual assertion
  • PMID:9646842
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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

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Last updated: April 7, 2025