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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 5801 - 5825 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence References
DOID:9352 type 2 diabetes mellitus HGNC:6126 Homo sapiens (human) 8660 IRS2 inference by association of genotype from phenotype used in manual assertion
  • PMID:11030756
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus HGNC:6125 Homo sapiens (human) 3667 IRS1 inference by association of genotype from phenotype used in manual assertion
  • PMID:12679424
  • PMID:14633864
  • RGD:7240710
DOID:10652 Alzheimer's disease HGNC:6125 Homo sapiens (human) 3667 IRS1 inference by association of genotype from phenotype used in manual assertion
  • PMID:24589556
DOID:13223 uterine fibroid HGNC:6125 Homo sapiens (human) 3667 IRS1 inference by association of genotype from phenotype used in manual assertion
  • PMID:23818951
DOID:3393 coronary artery disease HGNC:6125 Homo sapiens (human) 3667 IRS1 inference by association of genotype from phenotype used in manual assertion
  • PMID:10591678
DOID:0111969 immunodeficiency 39 HGNC:6122 Homo sapiens (human) 3665 IRF7 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:8566 herpes simplex HGNC:6120 Homo sapiens (human) 3663 IRF5 inference by association of genotype from phenotype used in manual assertion
  • PMID:20861862
DOID:0110895 inflammatory bowel disease 14 HGNC:6120 Homo sapiens (human) 3663 IRF5 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9074 systemic lupus erythematosus HGNC:6120 Homo sapiens (human) 3663 IRF5 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:7148 rheumatoid arthritis HGNC:6120 Homo sapiens (human) 3663 IRF5 direct assay evidence used in manual assertion
  • PMID:29352853
  • PMID:29379122
DOID:2377 multiple sclerosis HGNC:6120 Homo sapiens (human) 3663 IRF5 inference by association of genotype from phenotype used in manual assertion
  • PMID:20861862
DOID:2377 multiple sclerosis HGNC:6120 Homo sapiens (human) 3663 IRF5 direct assay evidence used in manual assertion
  • PMID:25392335
DOID:9970 obesity HGNC:612 Homo sapiens (human) 347 APOD inference by association of genotype from phenotype used in manual assertion
  • PMID:7913935
DOID:9352 type 2 diabetes mellitus HGNC:612 Homo sapiens (human) 347 APOD inference by association of genotype from phenotype used in manual assertion
  • PMID:7895459
DOID:0050749 peripheral T-cell lymphoma HGNC:6119 Homo sapiens (human) 3662 IRF4 inference by association of genotype from phenotype used in manual assertion
  • PMID:18987657
DOID:10123 pigmentation disease HGNC:6119 Homo sapiens (human) 3662 IRF4 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050744 anaplastic large cell lymphoma HGNC:6119 Homo sapiens (human) 3662 IRF4 inference by association of genotype from phenotype used in manual assertion
  • PMID:18987657
DOID:9952 acute lymphoblastic leukemia HGNC:6119 Homo sapiens (human) 3662 IRF4 inference by association of genotype from phenotype used in manual assertion
  • PMID:19897031
DOID:1040 chronic lymphocytic leukemia HGNC:6119 Homo sapiens (human) 3662 IRF4 inference by association of genotype from phenotype used in manual assertion
  • PMID:20090783
  • PMID:20123861
  • PMID:20731705
  • PMID:21791429
DOID:9538 multiple myeloma HGNC:6119 Homo sapiens (human) 3662 IRF4 inference by association of genotype from phenotype used in manual assertion
  • PMID:10557056
DOID:10652 Alzheimer's disease HGNC:6115 Homo sapiens (human) 3658 IREB2 inference by association of genotype from phenotype used in manual assertion
  • PMID:16914832
DOID:1580 diffuse scleroderma HGNC:6112 Homo sapiens (human) 3654 IRAK1 inference by association of genotype from phenotype used in manual assertion
  • PMID:21898345
DOID:7147 ankylosing spondylitis HGNC:6112 Homo sapiens (human) 3654 IRAK1 inference by association of genotype from phenotype used in manual assertion
  • PMID:20500689
DOID:9008 psoriatic arthritis HGNC:6112 Homo sapiens (human) 3654 IRAK1 inference by association of genotype from phenotype used in manual assertion
  • PMID:20500689
DOID:1749 squamous cell carcinoma HGNC:6112 Homo sapiens (human) 3654 IRAK1 mutant phenotype evidence used in manual assertion
  • PMID:24302991
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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