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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 10001 - 10025 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:6011 Homo sapiens (human) 3562 IL3 inference by association of genotype from phenotype used in manual assertion
  • PMID:15372320
  • PMID:24684517
DOID:12361 Graves' disease HGNC:6011 Homo sapiens (human) 3562 IL3 inference by association of genotype from phenotype used in manual assertion
  • PMID:20332709
DOID:7148 rheumatoid arthritis HGNC:6011 Homo sapiens (human) 3562 IL3 inference by association of genotype from phenotype used in manual assertion
  • PMID:20018070
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:8924 autoimmune thrombocytopenic purpura HGNC:6001 Homo sapiens (human) 3558 IL2 inference by association of genotype from phenotype used in manual assertion
  • PMID:20626741
DOID:11054 urinary bladder cancer HGNC:6001 Homo sapiens (human) 3558 IL2 direct assay evidence used in manual assertion
  • PMID:3262172
DOID:5520 head and neck squamous cell carcinoma HGNC:6001 Homo sapiens (human) 3558 IL2 direct assay evidence used in manual assertion
  • PMID:2787951
  • PMID:3263896
DOID:684 hepatocellular carcinoma HGNC:6001 Homo sapiens (human) 3558 IL2 direct assay evidence used in manual assertion
  • PMID:10933975
  • PMID:9449371
DOID:1884 viral hepatitis HGNC:6001 Homo sapiens (human) 3558 IL2 inference by association of genotype from phenotype used in manual assertion
  • PMID:21162873
DOID:2508 Takayasu's arteritis HGNC:6001 Homo sapiens (human) 3558 IL2 direct assay evidence used in manual assertion
  • PMID:2574087
DOID:0050866 oral squamous cell carcinoma HGNC:6001 Homo sapiens (human) 3558 IL2 direct assay evidence used in manual assertion
  • PMID:10389944
DOID:12361 Graves' disease HGNC:6001 Homo sapiens (human) 3558 IL2 direct assay evidence used in manual assertion
  • PMID:2279527
DOID:1749 squamous cell carcinoma HGNC:6001 Homo sapiens (human) 3558 IL2 direct assay evidence used in manual assertion
  • PMID:11023201
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Supported by JST NBDC Grant Number JPMJND2204

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Last updated: April 7, 2025