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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 July 29, 2024
Displaying entries 9801 - 9825 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:11650 bronchopulmonary dysplasia HGNC:2666 Homo sapiens (human) 1605 DAG1
  • PMID:17196572
DOID:3429 inclusion body myositis HGNC:2666 Homo sapiens (human) 1605 DAG1
  • PMID:14972325
DOID:12930 dilated cardiomyopathy HGNC:2666 Homo sapiens (human) 1605 DAG1
  • MGI:6194238
DOID:5844 myocardial infarction HGNC:2666 Homo sapiens (human) 1605 DAG1
  • MGI:6194238
DOID:0050588 muscular dystrophy-dystroglycanopathy type B1 HGNC:2666 Homo sapiens (human) 1605 DAG1
  • MGI:6194238
DOID:0110293 autosomal recessive limb-girdle muscular dystrophy type 2P HGNC:2666 Homo sapiens (human) 1605 DAG1
  • MGI:6194238
  • RGD:7240710
DOID:767 muscular atrophy HGNC:2666 Homo sapiens (human) 1605 DAG1
  • MGI:6194238
DOID:9884 muscular dystrophy HGNC:2666 Homo sapiens (human) 1605 DAG1
  • MGI:6194238
DOID:0112374 muscular dystrophy-dystroglycanopathy HGNC:2666 Homo sapiens (human) 1605 DAG1
  • MGI:6194238
DOID:0110278 autosomal recessive limb-girdle muscular dystrophy type 2D HGNC:2666 Homo sapiens (human) 1605 DAG1
  • PMID:15833425
DOID:0112315 brain small vessel disease 3 WB:WBGene00008426 Caenorhabditis elegans 3565069 D2045.9
  • MGI:6194238
DOID:5844 myocardial infarction FB:FBgn0261955 Drosophila melanogaster (fruit fly) 31579 Cs1
  • MGI:6194238
DOID:11984 hypertrophic cardiomyopathy FB:FBgn0261955 Drosophila melanogaster (fruit fly) 31579 Cs1
  • MGI:6194238
DOID:6000 congestive heart failure FB:FBgn0261955 Drosophila melanogaster (fruit fly) 31579 Cs1
  • MGI:6194238
DOID:3312 bipolar disorder FB:FBgn0261955 Drosophila melanogaster (fruit fly) 31579 Cs1
  • MGI:6194238
DOID:7998 hyperthyroidism FB:FBgn0261955 Drosophila melanogaster (fruit fly) 31579 Cs1
  • MGI:6194238
DOID:8466 retinal degeneration FB:FBgn0261955 Drosophila melanogaster (fruit fly) 31579 Cs1
  • PMID:26176594
DOID:12930 dilated cardiomyopathy FB:FBgn0261955 Drosophila melanogaster (fruit fly) 31579 Cs1
  • MGI:6194238
DOID:0050852 limb ischemia FB:FBgn0261955 Drosophila melanogaster (fruit fly) 31579 Cs1
  • MGI:6194238
DOID:1459 hypothyroidism FB:FBgn0261955 Drosophila melanogaster (fruit fly) 31579 Cs1
  • MGI:6194238
DOID:3312 bipolar disorder MGI:88529 Mus musculus (house mouse) 12974 Cs
  • MGI:6194238
DOID:8466 retinal degeneration MGI:88529 Mus musculus (house mouse) 12974 Cs
  • MGI:6194238
DOID:0050852 limb ischemia MGI:88529 Mus musculus (house mouse) 12974 Cs
  • MGI:6194238
DOID:11984 hypertrophic cardiomyopathy MGI:88529 Mus musculus (house mouse) 12974 Cs
  • MGI:6194238
DOID:3312 bipolar disorder RGD:620330 Rattus norvegicus (Norway rat) 170587 Cs
  • PMID:17367908
  • PMID:20372980
  • PMID:24359811

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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: August 19, 2024