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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 1 - 25 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▲ FlyGlycoDB Evidence References
DOID:14320 generalized anxiety disorder FB:FBgn0263116 Drosophila melanogaster (fruit fly) 37191 5-HT1B combinatorial experimental and author inference evidence used in manual assertion
  • PMID:27020741
DOID:14330 Parkinson's disease HGNC:7 Homo sapiens (human) 2 A2M inference by association of genotype from phenotype used in manual assertion
  • PMID:12133586
DOID:13208 background diabetic retinopathy HGNC:7 Homo sapiens (human) 2 A2M direct assay evidence used in manual assertion
  • PMID:10848441
DOID:2377 multiple sclerosis HGNC:7 Homo sapiens (human) 2 A2M inference by association of genotype from phenotype used in manual assertion
  • PMID:11498265
DOID:2320 obstructive lung disease HGNC:7 Homo sapiens (human) 2 A2M inference by association of genotype from phenotype used in manual assertion
  • PMID:2475424
DOID:10652 Alzheimer's disease HGNC:7 Homo sapiens (human) 2 A2M inference by association of genotype from phenotype used in manual assertion
  • PMID:12133586
  • PMID:12966032
  • PMID:14675603
  • PMID:9697696
DOID:0080600 COVID-19 HGNC:7 Homo sapiens (human) 2 A2M inference by association of genotype from phenotype used in manual assertion
  • PMID:32747830
DOID:10754 otitis media HGNC:23336 Homo sapiens (human) 144568 A2ML1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:14115 toxic shock syndrome RGD:2004 Rattus norvegicus (Norway rat) 24153 A2m direct assay evidence used in manual assertion
  • PMID:2424486
DOID:583 hemolytic anemia RGD:2004 Rattus norvegicus (Norway rat) 24153 A2m direct assay evidence used in manual assertion
  • PMID:11952820
DOID:9164 achalasia HGNC:13666 Homo sapiens (human) 8086 AAAS inference by association of genotype from phenotype used in manual assertion
  • PMID:16098009
DOID:0050602 triple-A syndrome HGNC:13666 Homo sapiens (human) 8086 AAAS inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:10579 leukodystrophy HGNC:20 Homo sapiens (human) 16 AARS1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110177 Charcot-Marie-Tooth disease axonal type 2N HGNC:20 Homo sapiens (human) 16 AARS1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111866 trichothiodystrophy HGNC:20 Homo sapiens (human) 16 AARS1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080451 developmental and epileptic encephalopathy 29 HGNC:20 Homo sapiens (human) 16 AARS1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0070396 progressive leukoencephalopathy with ovarian failure HGNC:21022 Homo sapiens (human) 57505 AARS2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111479 combined oxidative phosphorylation deficiency 8 HGNC:21022 Homo sapiens (human) 57505 AARS2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:10652 Alzheimer's disease HGNC:23 Homo sapiens (human) 18 ABAT direct assay evidence used in manual assertion
  • PMID:1627256
DOID:12858 Huntington's disease HGNC:23 Homo sapiens (human) 18 ABAT direct assay evidence used in manual assertion
  • PMID:6237280
DOID:0060174 GABA aminotransferase deficiency HGNC:23 Homo sapiens (human) 18 ABAT inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9970 obesity HGNC:29 Homo sapiens (human) 19 ABCA1 inference by association of genotype from phenotype used in manual assertion
  • PMID:17287470
DOID:10652 Alzheimer's disease HGNC:29 Homo sapiens (human) 19 ABCA1 inference by association of genotype from phenotype used in manual assertion
  • PMID:15024730
DOID:3393 coronary artery disease HGNC:29 Homo sapiens (human) 19 ABCA1 inference by association of genotype from phenotype used in manual assertion
  • PMID:11086027
DOID:9352 type 2 diabetes mellitus HGNC:29 Homo sapiens (human) 19 ABCA1 inference by association of genotype from phenotype used in manual assertion
  • PMID:18003760
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: April 7, 2025