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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 13276 - 13300 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence References ▼
DOID:9744 type 1 diabetes mellitus HGNC:1653 Homo sapiens (human) 940 CD28 inference by association of genotype from phenotype used in manual assertion
  • PMID:11685455
DOID:4195 hyperglycemia RGD:620630 Rattus norvegicus (Norway rat) 85268 Hrh3 direct assay evidence used in manual assertion
  • PMID:11684344
DOID:10763 hypertension RGD:69051 Rattus norvegicus (Norway rat) 59086 Tgfb1 inference by association of genotype from phenotype used in manual assertion
  • PMID:11682445
DOID:0080056 achondrogenesis type II MGI:88452 Mus musculus (house mouse) 12824 Col2a1 author statement supported by traceable reference
  • PMID:11680679
DOID:12361 Graves' disease HGNC:4951 Homo sapiens (human) 3125 HLA-DRB3 inference by association of genotype from phenotype used in manual assertion
  • PMID:11678832
DOID:299 adenocarcinoma HGNC:583 Homo sapiens (human) 324 APC inference by association of genotype from phenotype used in manual assertion
  • PMID:11677205
DOID:657 adenoma HGNC:583 Homo sapiens (human) 324 APC inference by association of genotype from phenotype used in manual assertion
  • PMID:11677205
DOID:3310 atopic dermatitis MGI:96556 Mus musculus (house mouse) 16189 Il4 author statement supported by traceable reference
  • PMID:11676841
DOID:2959 hyperimmunoglobulin syndrome HGNC:11919 Homo sapiens (human) 958 CD40 inference by association of genotype from phenotype used in manual assertion
  • PMID:11675497
DOID:10763 hypertension RGD:2521 Rattus norvegicus (Norway rat) 29238 Drd3 direct assay evidence used in manual assertion
  • PMID:11675403
DOID:2841 asthma HGNC:3176 Homo sapiens (human) 1906 EDN1 inference by association of genotype from phenotype used in manual assertion
  • PMID:11668616
DOID:12801 mucopolysaccharidosis III HGNC:7632 Homo sapiens (human) 4669 NAGLU inference by association of genotype from phenotype used in manual assertion
  • PMID:11668611
DOID:0080026 otospondylomegaepiphyseal dysplasia, autosomal recessive MGI:88447 Mus musculus (house mouse) 12815 Col11a2 author statement supported by traceable reference
  • PMID:11668593
DOID:0110545 autosomal dominant nonsyndromic deafness 13 MGI:88447 Mus musculus (house mouse) 12815 Col11a2 author statement supported by traceable reference
  • PMID:11668593
DOID:0080046 Stickler syndrome MGI:88447 Mus musculus (house mouse) 12815 Col11a2 author statement supported by traceable reference
  • PMID:11668593
DOID:6000 congestive heart failure RGD:3876 Rattus norvegicus (Norway rat) 24835 Tnf mutant phenotype evidence used in manual assertion
  • PMID:11668085
  • PMID:15210453
DOID:13359 Ehlers-Danlos syndrome HGNC:11976 Homo sapiens (human) 7148 TNXB inference by association of genotype from phenotype used in manual assertion
  • PMID:11642233
DOID:9074 systemic lupus erythematosus HGNC:11892 Homo sapiens (human) 7124 TNF inference by association of genotype from phenotype used in manual assertion
  • PMID:11607787
DOID:3007 breast ductal carcinoma HGNC:971 Homo sapiens (human) 9564 BCAR1 direct assay evidence used in manual assertion
  • PMID:11605729
DOID:0050902 medulloblastoma HGNC:12363 Homo sapiens (human) 7249 TSC2 inference by association of genotype from phenotype used in manual assertion
  • PMID:11603814
DOID:4184 pseudohypoparathyroidism HGNC:4392 Homo sapiens (human) 2778 GNAS direct assay evidence used in manual assertion
  • PMID:11600516
  • PMID:18812479
DOID:3526 cerebral infarction HGNC:2707 Homo sapiens (human) 1636 ACE inference by association of genotype from phenotype used in manual assertion
  • PMID:11596779
DOID:1793 pancreatic cancer HGNC:391 Homo sapiens (human) 207 AKT1 direct assay evidence used in manual assertion
  • PMID:11595724
DOID:397 restrictive cardiomyopathy HGNC:6843 Homo sapiens (human) 5606 MAP2K3 mutant phenotype evidence used in manual assertion
  • PMID:11593045
DOID:397 restrictive cardiomyopathy HGNC:6846 Homo sapiens (human) 5608 MAP2K6 mutant phenotype evidence used in manual assertion
  • PMID:11593045
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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: December 8, 2025