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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 5726 - 5750 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence References
DOID:5419 schizophrenia HGNC:6144 Homo sapiens (human) 8516 ITGA8 inference by association of genotype from phenotype used in manual assertion
  • PMID:23153507
DOID:783 end stage renal disease HGNC:6144 Homo sapiens (human) 8516 ITGA8 inference by association of genotype from phenotype used in manual assertion
  • PMID:18277079
DOID:11723 Duchenne muscular dystrophy HGNC:6143 Homo sapiens (human) 3679 ITGA7 mutant phenotype evidence used in manual assertion
  • PMID:23319059
DOID:0080000 muscular disease HGNC:6143 Homo sapiens (human) 3679 ITGA7 inference by association of genotype from phenotype used in manual assertion
  • PMID:9590299
DOID:0110639 congenital muscular dystrophy due to integrin alpha-7 deficiency HGNC:6143 Homo sapiens (human) 3679 ITGA7 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0060733 junctional epidermolysis bullosa with pyloric atresia HGNC:6142 Homo sapiens (human) 3655 ITGA6 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3209 junctional epidermolysis bullosa HGNC:6142 Homo sapiens (human) 3655 ITGA6 inference by association of genotype from phenotype used in manual assertion
  • PMID:9185503
DOID:0060041 autism spectrum disorder HGNC:6140 Homo sapiens (human) 3676 ITGA4 inference by association of genotype from phenotype used in manual assertion
  • PMID:19259978
DOID:1793 pancreatic cancer HGNC:6140 Homo sapiens (human) 3676 ITGA4 inference by association of genotype from phenotype used in manual assertion
  • PMID:18772397
DOID:3209 junctional epidermolysis bullosa HGNC:6139 Homo sapiens (human) 3675 ITGA3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:2219 Glanzmann's thrombasthenia HGNC:6138 Homo sapiens (human) 3674 ITGA2B inference by association of genotype from phenotype used in manual assertion
  • PMID:7529063
  • PMID:8111043
  • RGD:7240710
DOID:0060691 platelet-type bleeding disorder 16 HGNC:6138 Homo sapiens (human) 3674 ITGA2B inference by association of genotype from phenotype used in manual assertion
  • PMID:19691478
  • PMID:21029361
  • PMID:22394243
  • RGD:7240710
DOID:1588 thrombocytopenia HGNC:6138 Homo sapiens (human) 3674 ITGA2B inference by association of genotype from phenotype used in manual assertion
  • PMID:21454453
DOID:0060573 von Willebrand's disease 1 HGNC:6138 Homo sapiens (human) 3674 ITGA2B inference by association of genotype from phenotype used in manual assertion
  • PMID:15226188
DOID:0060573 von Willebrand's disease 1 HGNC:6137 Homo sapiens (human) 3673 ITGA2 inference by association of genotype from phenotype used in manual assertion
  • PMID:15226188
DOID:0060903 thrombosis HGNC:6137 Homo sapiens (human) 3673 ITGA2 inference by association of genotype from phenotype used in manual assertion
  • PMID:12412731
DOID:2219 Glanzmann's thrombasthenia HGNC:6137 Homo sapiens (human) 3673 ITGA2 inference by association of genotype from phenotype used in manual assertion
  • PMID:14687991
DOID:2349 arteriosclerosis HGNC:6137 Homo sapiens (human) 3673 ITGA2 inference by association of genotype from phenotype used in manual assertion
  • PMID:11978651
DOID:9351 diabetes mellitus HGNC:6137 Homo sapiens (human) 3673 ITGA2 direct assay evidence used in manual assertion
  • PMID:17466965
DOID:1588 thrombocytopenia HGNC:6137 Homo sapiens (human) 3673 ITGA2 inference by association of genotype from phenotype used in manual assertion
  • PMID:22133274
DOID:9352 type 2 diabetes mellitus HGNC:6137 Homo sapiens (human) 3673 ITGA2 direct assay evidence used in manual assertion
  • PMID:15025679
DOID:0060574 von Willebrand's disease 2 HGNC:6137 Homo sapiens (human) 3673 ITGA2 inference by association of genotype from phenotype used in manual assertion
  • PMID:16409463
DOID:13241 Behcet's disease HGNC:6137 Homo sapiens (human) 3673 ITGA2 inference by association of genotype from phenotype used in manual assertion
  • PMID:12412731
DOID:5844 myocardial infarction HGNC:6137 Homo sapiens (human) 3673 ITGA2 inference by association of genotype from phenotype used in manual assertion
  • PMID:10194421
  • PMID:16697311
DOID:8805 intermediate coronary syndrome HGNC:6137 Homo sapiens (human) 3673 ITGA2 inference by association of genotype from phenotype used in manual assertion
  • PMID:15104219
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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