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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 13501 - 13525 of 14279 in total
Disease ID Disease Name ▲ Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence References
DOID:1588 thrombocytopenia HGNC:3749 Homo sapiens (human) 2313 FLI1 inference by association of genotype from phenotype used in manual assertion
  • PMID:15232614
DOID:1588 thrombocytopenia HGNC:6922 Homo sapiens (human) 4153 MBL2 inference by association of genotype from phenotype used in manual assertion
  • PMID:18361938
DOID:1588 thrombocytopenia HGNC:4036 Homo sapiens (human) 2533 FYB1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:1588 thrombocytopenia HGNC:11283 Homo sapiens (human) 6714 SRC inference by association of genotype from phenotype used in manual assertion
  • 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:1587 thrombocytopenia due to platelet alloimmunization HGNC:3619 Homo sapiens (human) 2214 FCGR3A inference by association of genotype from phenotype used in manual assertion
  • PMID:22775462
DOID:2228 thrombocytosis HGNC:1455 Homo sapiens (human) 811 CALR inference by association of genotype from phenotype used in manual assertion
  • PMID:26608331
DOID:2228 thrombocytosis HGNC:11795 Homo sapiens (human) 7066 THPO inference by association of genotype from phenotype used in manual assertion
  • PMID:9694695
DOID:2228 thrombocytosis HGNC:7217 Homo sapiens (human) 4352 MPL inference by association of genotype from phenotype used in manual assertion
  • PMID:19036112
  • RGD:7240710
DOID:2452 thrombophilia MGI:98736 Mus musculus (house mouse) 21824 Thbd author statement supported by traceable reference
  • PMID:12208873
DOID:2452 thrombophilia HGNC:4942 Homo sapiens (human) 3117 HLA-DQA1 inference by association of genotype from phenotype used in manual assertion
  • PMID:23454623
DOID:2452 thrombophilia HGNC:9451 Homo sapiens (human) 5624 PROC inference by association of genotype from phenotype used in manual assertion
  • PMID:2437584
  • PMID:7881411
DOID:2452 thrombophilia HGNC:3661 Homo sapiens (human) 2243 FGA inference by association of genotype from phenotype used in manual assertion
  • PMID:10910940
DOID:2452 thrombophilia HGNC:9451 Homo sapiens (human) 5624 PROC direct assay evidence used in manual assertion
  • PMID:24189967
DOID:2452 thrombophilia HGNC:9071 Homo sapiens (human) 5340 PLG inference by association of genotype from phenotype used in manual assertion
  • PMID:8392398
DOID:2452 thrombophilia HGNC:15996 Homo sapiens (human) 51156 SERPINA10 inference by association of genotype from phenotype used in manual assertion
  • PMID:15461625
DOID:0111903 thrombophilia due to HRG deficiency HGNC:5181 Homo sapiens (human) 3273 HRG inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111902 thrombophilia due to activated protein C resistance HGNC:3542 Homo sapiens (human) 2153 F5 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111902 thrombophilia due to activated protein C resistance HGNC:9451 Homo sapiens (human) 5624 PROC direct assay evidence used in manual assertion
  • PMID:25196808
DOID:0111907 thrombophilia due to thrombin defect HGNC:4798 Homo sapiens (human) 3026 HABP2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111907 thrombophilia due to thrombin defect HGNC:3531 Homo sapiens (human) 2162 F13A1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111907 thrombophilia due to thrombin defect HGNC:3535 Homo sapiens (human) 2147 F2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111908 thrombophilia due to thrombomodulin defect HGNC:11784 Homo sapiens (human) 7056 THBD inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3875 thrombophlebitis HGNC:4932 Homo sapiens (human) 3106 HLA-B inference by association of genotype from phenotype used in manual assertion
  • PMID:12372094
DOID:0060903 thrombosis HGNC:5181 Homo sapiens (human) 3273 HRG inference by association of genotype from phenotype used in manual assertion
  • PMID:9414276
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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: December 8, 2025