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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 6001 - 6025 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence References
DOID:0081120 Graves ophthalmopathy HGNC:6011 Homo sapiens (human) 3562 IL3 inference by association of genotype from phenotype used in manual assertion
  • PMID:20332709
DOID:628 combined T cell and B cell immunodeficiency HGNC:6010 Homo sapiens (human) 3561 IL2RG inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0060013 X-linked severe combined immunodeficiency HGNC:6010 Homo sapiens (human) 3561 IL2RG inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:627 severe combined immunodeficiency HGNC:6010 Homo sapiens (human) 3561 IL2RG inference by association of genotype from phenotype used in manual assertion
  • PMID:7557965
DOID:437 myasthenia gravis HGNC:6009 Homo sapiens (human) 3560 IL2RB inference by association of genotype from phenotype used in manual assertion
  • PMID:20728947
DOID:2841 asthma HGNC:6009 Homo sapiens (human) 3560 IL2RB inference by association of genotype from phenotype used in manual assertion
  • PMID:20860503
DOID:0111997 immunodeficiency 63 HGNC:6009 Homo sapiens (human) 3560 IL2RB inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9146 visceral leishmaniasis HGNC:6009 Homo sapiens (human) 3560 IL2RB inference by association of genotype from phenotype used in manual assertion
  • PMID:17108990
DOID:9744 type 1 diabetes mellitus HGNC:6008 Homo sapiens (human) 3559 IL2RA inference by association of genotype from phenotype used in manual assertion
  • PMID:19106270
  • PMID:19119414
DOID:614 lymphopenia HGNC:6008 Homo sapiens (human) 3559 IL2RA inference by association of genotype from phenotype used in manual assertion
  • PMID:9096364
DOID:0111968 immunodeficiency 41 HGNC:6008 Homo sapiens (human) 3559 IL2RA inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110749 type 1 diabetes mellitus 10 HGNC:6008 Homo sapiens (human) 3559 IL2RA inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:2377 multiple sclerosis HGNC:6008 Homo sapiens (human) 3559 IL2RA inference by association of genotype from phenotype used in manual assertion
  • PMID:19125193
DOID:526 human immunodeficiency virus infectious disease HGNC:6006 Homo sapiens (human) 50615 IL21R direct assay evidence used in manual assertion
  • PMID:22530560
DOID:9074 systemic lupus erythematosus HGNC:6006 Homo sapiens (human) 50615 IL21R inference by association of genotype from phenotype used in manual assertion
  • PMID:19644854
DOID:13375 temporal arteritis HGNC:6006 Homo sapiens (human) 50615 IL21R direct assay evidence used in manual assertion
  • PMID:22147555
DOID:2377 multiple sclerosis HGNC:6006 Homo sapiens (human) 50615 IL21R inference by association of genotype from phenotype used in manual assertion
  • PMID:20072140
DOID:12177 common variable immunodeficiency HGNC:6006 Homo sapiens (human) 50615 IL21R inference by association of genotype from phenotype used in manual assertion
  • PMID:18254984
DOID:0111982 immunodeficiency 56 HGNC:6006 Homo sapiens (human) 50615 IL21R inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050745 diffuse large B-cell lymphoma HGNC:6006 Homo sapiens (human) 50615 IL21R inference by association of genotype from phenotype used in manual assertion
  • PMID:11821949
DOID:13241 Behcet's disease HGNC:6006 Homo sapiens (human) 50615 IL21R mutant phenotype evidence used in manual assertion
  • PMID:21724243
DOID:707 B-cell lymphoma HGNC:6006 Homo sapiens (human) 50615 IL21R inference by association of genotype from phenotype used in manual assertion
  • PMID:11821949
DOID:8778 Crohn's disease HGNC:6006 Homo sapiens (human) 50615 IL21R inference by association of genotype from phenotype used in manual assertion
  • PMID:22021194
DOID:2841 asthma HGNC:6005 Homo sapiens (human) 59067 IL21 inference by association of genotype from phenotype used in manual assertion
  • PMID:18802358
DOID:9074 systemic lupus erythematosus HGNC:6005 Homo sapiens (human) 59067 IL21 inference by association of genotype from phenotype used in manual assertion
  • PMID:23236436
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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

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Last updated: April 7, 2025