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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 76 - 100 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▲ Evidence References
DOID:0060438 Cole-Carpenter syndrome HGNC:10706 Homo sapiens (human) 9871 SEC24D inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0060072 benign neoplasm FB:FBgn0263289 Drosophila melanogaster (fruit fly) 44448 scrib combinatorial experimental and author inference evidence used in manual assertion
  • PMID:29870719
DOID:0070355 overactive bladder syndrome RGD:1598328 Rattus norvegicus (Norway rat) 310738 Ngf direct assay evidence used in manual assertion
  • PMID:21605172
  • PMID:22473863
DOID:0110035 Alzheimer's disease 2 HGNC:613 Homo sapiens (human) 348 APOE inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:891 progressive myoclonus epilepsy MGI:1196458 Mus musculus (house mouse) 12492 Scarb2 author statement supported by traceable reference
  • PMID:25316793
DOID:0080855 Parkinsonism RGD:3684 Rattus norvegicus (Norway rat) 25715 Slc11a2 direct assay evidence used in manual assertion
  • PMID:20125122
DOID:12120 pulmonary alveolar proteinosis HGNC:2436 Homo sapiens (human) 1439 CSF2RB inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050650 familial atrial fibrillation HGNC:10593 Homo sapiens (human) 6331 SCN5A inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:12858 Huntington's disease WB:WBGene00018294 Caenorhabditis elegans 179246 atg-18 combinatorial experimental and author inference evidence used in manual assertion
  • PMID:17172799
DOID:9256 colorectal cancer HGNC:2731 Homo sapiens (human) 4921 DDR2 direct assay evidence used in manual assertion
  • PMID:28476831
DOID:14018 alcoholic liver cirrhosis HGNC:404 Homo sapiens (human) 217 ALDH2 inference by association of genotype from phenotype used in manual assertion
  • PMID:11051375
  • PMID:23550892
  • PMID:29779728
DOID:1574 alcohol use disorder RGD:61800 Rattus norvegicus (Norway rat) 29595 Htr2a mutant phenotype evidence used in manual assertion
  • PMID:9631953
DOID:0050641 Rh deficiency syndrome HGNC:10006 Homo sapiens (human) 6005 RHAG inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:1875 impotence RGD:620103 Rattus norvegicus (Norway rat) 64639 Bad direct assay evidence used in manual assertion
  • PMID:21235725
DOID:0060455 Thiel-Behnke corneal dystrophy HGNC:11771 Homo sapiens (human) 7045 TGFBI inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:10632 Wolfram syndrome HGNC:12762 Homo sapiens (human) 7466 WFS1 inference by association of genotype from phenotype used in manual assertion
  • PMID:9771706
DOID:0090125 brain small vessel disease 1 MGI:88454 Mus musculus (house mouse) 12826 Col4a1 author statement supported by traceable reference
  • PMID:16598045
DOID:5844 myocardial infarction RGD:3249 Rattus norvegicus (Norway rat) 24617 Serpine1 mutant phenotype evidence used in manual assertion
  • PMID:16053971
DOID:4989 pancreatitis RGD:61800 Rattus norvegicus (Norway rat) 29595 Htr2a direct assay evidence used in manual assertion
  • PMID:16183055
DOID:2741 bilirubin metabolic disorder HGNC:10961 Homo sapiens (human) 28234 SLCO1B3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:11054 urinary bladder cancer MGI:88276 Mus musculus (house mouse) 12387 Ctnnb1 author statement supported by traceable reference
  • PMID:23928991
DOID:0070042 Coffin-Siris syndrome 1 HGNC:18040 Homo sapiens (human) 57492 ARID1B inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:11198 DiGeorge syndrome MGI:104686 Mus musculus (house mouse) 12929 Crkl author statement supported by traceable reference
  • PMID:11242111
DOID:9352 type 2 diabetes mellitus HGNC:5233 Homo sapiens (human) 3304 HSPA1B inference by association of genotype from phenotype used in manual assertion
  • PMID:15223990
DOID:2394 ovarian cancer HGNC:10473 Homo sapiens (human) 864 RUNX3 direct assay evidence used in manual assertion
  • PMID:26175272
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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