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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 13476 - 13500 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▲ Evidence References
DOID:10763 hypertension RGD:2072 Rattus norvegicus (Norway rat) 24182 Agtr2 mutant phenotype evidence used in manual assertion
  • PMID:19680135
  • PMID:21040717
DOID:0110914 infantile hypophosphatasia SGD:S000002889 Saccharomyces cerevisiae S288C 852092 PHO8 sequence similarity evidence used in manual assertion
  • PMID:25860149
DOID:0111052 Scott syndrome HGNC:25240 Homo sapiens (human) 196527 ANO6 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:1171 hyperlipoproteinemia type V HGNC:17288 Homo sapiens (human) 116519 APOA5 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3908 lung non-small cell carcinoma HGNC:3467 Homo sapiens (human) 2099 ESR1 direct assay evidence used in manual assertion
  • PMID:19506903
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:13100 intracranial vasospasm HGNC:10483 Homo sapiens (human) 6261 RYR1 inference by association of genotype from phenotype used in manual assertion
  • PMID:21503806
DOID:9352 type 2 diabetes mellitus HGNC:9291 Homo sapiens (human) 5506 PPP1R3A mutant phenotype evidence used in manual assertion
  • PMID:11793847
DOID:0060298 complement component 4b deficiency HGNC:1324 Homo sapiens (human) 721 C4B inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:988 mitral valve prolapse MGI:2685011 Mus musculus (house mouse) 233651 Dchs1 author statement supported by traceable reference
  • PMID:26258302
DOID:0112223 developmental and epileptic encephalopathy 89 HGNC:4092 Homo sapiens (human) 2571 GAD1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:2058 chronic mucocutaneous candidiasis HGNC:18358 Homo sapiens (human) 84818 IL17RC inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110013 advanced sleep phase syndrome 3 HGNC:8847 Homo sapiens (human) 8863 PER3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:1612 breast cancer HGNC:1748 Homo sapiens (human) 999 CDH1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9976 heroin dependence HGNC:7978 Homo sapiens (human) 2908 NR3C1 inference by association of genotype from phenotype used in manual assertion
  • PMID:29465008
DOID:10763 hypertension RGD:3732 Rattus norvegicus (Norway rat) 24787 Sod2 direct assay evidence used in manual assertion
  • PMID:16716903
DOID:10763 hypertension HGNC:5141 Homo sapiens (human) 3240 HP inference by association of genotype from phenotype used in manual assertion
  • PMID:7606649
  • PMID:8228210
DOID:0060651 MYH-9 related disease MGI:107717 Mus musculus (house mouse) 17886 Myh9 author statement supported by traceable reference
  • PMID:21908426
DOID:10763 hypertension HGNC:19012 Homo sapiens (human) 10699 CORIN inference by association of genotype from phenotype used in manual assertion
  • PMID:16216958
  • PMID:17485366
DOID:0060041 autism spectrum disorder FB:FBgn0266557 Drosophila melanogaster (fruit fly) 33185 kis combinatorial experimental and author inference evidence used in manual assertion
  • PMID:32609087
  • PMID:34088660
DOID:13543 hyperparathyroidism HGNC:1514 Homo sapiens (human) 846 CASR inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:2841 asthma HGNC:6000 Homo sapiens (human) 3557 IL1RN mutant phenotype evidence used in manual assertion
  • PMID:16724092
DOID:13141 uveitis HGNC:11892 Homo sapiens (human) 7124 TNF mutant phenotype evidence used in manual assertion
  • PMID:20673052
DOID:1852 intrahepatic cholestasis HGNC:18324 Homo sapiens (human) 80270 HSD3B7 inference by association of genotype from phenotype used in manual assertion
  • PMID:12679481
DOID:14323 Marfan syndrome WB:WBGene00003482 Caenorhabditis elegans 176430 mua-3 mutant phenotype evidence used in manual assertion
  • PMID:25917920

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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