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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 6076 - 6100 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence References ▲
DOID:2841 asthma RGD:2886 Rattus norvegicus (Norway rat) 25325 Il10 genetic interaction evidence used in manual assertion
  • PMID:20560982
DOID:9351 diabetes mellitus MGI:99698 Mus musculus (house mouse) 12753 Clock author statement supported by traceable reference
  • PMID:20562852
DOID:2986 IgA glomerulonephritis HGNC:8784 Homo sapiens (human) 8654 PDE5A inference by association of genotype from phenotype used in manual assertion
  • PMID:20563733
DOID:0090142 cystathioninuria MGI:1339968 Mus musculus (house mouse) 107869 Cth author statement supported by traceable reference
  • PMID:20566639
DOID:8947 diabetic retinopathy RGD:620925 Rattus norvegicus (Norway rat) 83516 Ppargc1a direct assay evidence used in manual assertion
  • PMID:20566666
DOID:5082 liver cirrhosis HGNC:6922 Homo sapiens (human) 4153 MBL2 inference by association of genotype from phenotype used in manual assertion
  • PMID:20570631
  • PMID:26857650
DOID:1596 depressive disorder RGD:3184 Rattus norvegicus (Norway rat) 24598 Nos1 direct assay evidence used in manual assertion
  • PMID:20571741
DOID:150 disease of mental health MGI:109355 Mus musculus (house mouse) 20907 Stx1a author statement supported by traceable reference
  • PMID:20576034
DOID:10534 stomach cancer HGNC:4555 Homo sapiens (human) 2878 GPX3 inference by association of genotype from phenotype used in manual assertion
  • PMID:20576521
  • PMID:30114685
DOID:4448 macular degeneration HGNC:1228 Homo sapiens (human) 710 SERPING1 inference by association of genotype from phenotype used in manual assertion
  • PMID:20576771
  • PMID:20606025
DOID:2602 chondroma HGNC:9644 Homo sapiens (human) 5781 PTPN11 inference by association of genotype from phenotype used in manual assertion
  • PMID:20577567
DOID:3969 papillary thyroid carcinoma HGNC:12755 Homo sapiens (human) 10885 WDR3 inference by association of genotype from phenotype used in manual assertion
  • PMID:20578902
DOID:8924 autoimmune thrombocytopenic purpura HGNC:1705 Homo sapiens (human) 942 CD86 direct assay evidence used in manual assertion
  • PMID:20581660
DOID:0080855 Parkinsonism RGD:620144 Rattus norvegicus (Norway rat) 59109 Ntrk1 direct assay evidence used in manual assertion
  • PMID:20581854
DOID:12930 dilated cardiomyopathy MGI:1921256 Mus musculus (house mouse) 74006 Dnm1l author statement supported by traceable reference
  • PMID:20585624
DOID:9743 diabetic neuropathy RGD:620401 Rattus norvegicus (Norway rat) 81509 Bdkrb1 mutant phenotype evidence used in manual assertion
  • PMID:20587056
DOID:1324 lung cancer HGNC:1959 Homo sapiens (human) 1138 CHRNA5 inference by association of genotype from phenotype used in manual assertion
  • PMID:20587604
  • PMID:21448929
  • PMID:29193083
  • PMID:29993116
  • PMID:33419953
  • RGD:7240710
DOID:1324 lung cancer HGNC:1964 Homo sapiens (human) 1143 CHRNB4 inference by association of genotype from phenotype used in manual assertion
  • PMID:20587604
  • PMID:29416783
DOID:0060574 von Willebrand's disease 2 HGNC:12726 Homo sapiens (human) 7450 VWF mutant phenotype evidence used in manual assertion
  • PMID:20589313
DOID:0080379 nephrotic syndrome type 2 HGNC:17175 Homo sapiens (human) 51196 PLCE1 inference by association of genotype from phenotype used in manual assertion
  • PMID:20591883
DOID:2378 relapsing-remitting multiple sclerosis HGNC:5331 Homo sapiens (human) 64127 NOD2 inference by association of genotype from phenotype used in manual assertion
  • PMID:20595247
DOID:5844 myocardial infarction RGD:621576 Rattus norvegicus (Norway rat) 83531 Vdac2 direct assay evidence used in manual assertion
  • PMID:20601275
DOID:13241 Behcet's disease HGNC:11892 Homo sapiens (human) 7124 TNF mutant phenotype evidence used in manual assertion
  • PMID:20601837
DOID:1679 cystitis RGD:620349 Rattus norvegicus (Norway rat) 29527 Ptgs2 mutant phenotype evidence used in manual assertion
  • PMID:20602232
DOID:11123 IgA vasculitis HGNC:6998 Homo sapiens (human) 4210 MEFV inference by association of genotype from phenotype used in manual assertion
  • PMID:20602240
  • PMID:22451026
  • PMID:25232290

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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