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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 5926 - 5950 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▼ Evidence References
DOID:0080827 human cytomegalovirus infection HGNC:6340 Homo sapiens (human) 3813 KIR3DS1 inference by association of genotype from phenotype used in manual assertion
  • PMID:25253288
DOID:2513 basal cell carcinoma HGNC:8101 Homo sapiens (human) 4948 OCA2 inference by association of genotype from phenotype used in manual assertion
  • PMID:19384953
  • PMID:21270109
DOID:684 hepatocellular carcinoma HGNC:11730 Homo sapiens (human) 7015 TERT direct assay evidence used in manual assertion
  • PMID:25683523
DOID:10772 thrombotic thrombocytopenic purpura HGNC:1366 Homo sapiens (human) 11093 ADAMTS13 inference by association of genotype from phenotype used in manual assertion
  • PMID:11586351
  • PMID:18031293
  • RGD:7240710
DOID:1883 hepatitis C HGNC:4964 Homo sapiens (human) 3135 HLA-G inference by association of genotype from phenotype used in manual assertion
  • PMID:19775370
DOID:6432 pulmonary hypertension HGNC:11766 Homo sapiens (human) 7040 TGFB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:18496036
DOID:0050861 colorectal adenocarcinoma HGNC:5980 Homo sapiens (human) 3603 IL16 inference by association of genotype from phenotype used in manual assertion
  • PMID:27354594
DOID:0050458 juvenile myelomonocytic leukemia MGI:95559 Mus musculus (house mouse) 14255 Flt3 author statement supported by traceable reference
  • PMID:17936561
DOID:0060645 chronic recurrent multifocal osteomyelitis HGNC:14450 Homo sapiens (human) 9663 LPIN2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:13543 hyperparathyroidism MGI:1351351 Mus musculus (house mouse) 12374 Casr author statement supported by traceable reference
  • PMID:22527485
DOID:3429 inclusion body myositis HGNC:11180 Homo sapiens (human) 6648 SOD2 direct assay evidence used in manual assertion
  • PMID:11837748
DOID:670 amphetamine abuse HGNC:2228 Homo sapiens (human) 1312 COMT inference by association of genotype from phenotype used in manual assertion
  • PMID:15274053
  • PMID:17187009
  • PMID:21934638
  • PMID:33544778
DOID:14018 alcoholic liver cirrhosis HGNC:2631 Homo sapiens (human) 1571 CYP2E1 mutant phenotype evidence used in manual assertion
  • PMID:29404441
DOID:3827 congenital diaphragmatic hernia HGNC:15472 Homo sapiens (human) 8854 ALDH1A2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:7188 autoimmune thyroiditis HGNC:6694 Homo sapiens (human) 4036 LRP2 direct assay evidence used in manual assertion
  • PMID:10404822
DOID:13809 familial combined hyperlipidemia HGNC:6677 Homo sapiens (human) 4023 LPL inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:5844 myocardial infarction HGNC:3415 Homo sapiens (human) 2056 EPO direct assay evidence used in manual assertion
  • PMID:21415704
DOID:0080592 Klippel-Feil syndrome 4 HGNC:18150 Homo sapiens (human) 84700 MYO18B inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0090031 D-bifunctional protein deficiency MGI:105089 Mus musculus (house mouse) 15488 Hsd17b4 author statement supported by traceable reference
  • PMID:10748062
  • PMID:15769750
DOID:1612 breast cancer HGNC:5975 Homo sapiens (human) 3598 IL13RA2 mutant phenotype evidence used in manual assertion
  • PMID:11748276
  • PMID:17438063
DOID:11105 fundus albipunctatus HGNC:10024 Homo sapiens (human) 6017 RLBP1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:552 pneumonia HGNC:2707 Homo sapiens (human) 1636 ACE mutant phenotype evidence used in manual assertion
  • PMID:19455553
  • PMID:20051911
DOID:3021 acute kidney failure RGD:3870 Rattus norvegicus (Norway rat) 29260 Tlr4 direct assay evidence used in manual assertion
  • PMID:22266601
DOID:3627 aortic aneurysm MGI:1891209 Mus musculus (house mouse) 58859 Efemp2 author statement supported by traceable reference
  • PMID:23636094
DOID:3525 middle cerebral artery infarction RGD:620103 Rattus norvegicus (Norway rat) 64639 Bad direct assay evidence used in manual assertion
  • PMID:21891976
  • PMID:22200499

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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: December 8, 2025