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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 9951 - 9975 of 14279 in total
Disease ID Disease Name ▲ Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence References
DOID:8692 myeloid leukemia HGNC:4171 Homo sapiens (human) 2624 GATA2 inference by association of genotype from phenotype used in manual assertion
  • PMID:19304323
DOID:0070004 myeloid neoplasm HGNC:3688 Homo sapiens (human) 2260 FGFR1 mutant phenotype evidence used in manual assertion
  • PMID:12969958
  • PMID:15448205
DOID:0070004 myeloid neoplasm HGNC:1541 Homo sapiens (human) 867 CBL inference by association of genotype from phenotype used in manual assertion
  • PMID:19387008
  • PMID:22315494
DOID:0070004 myeloid neoplasm HGNC:4553 Homo sapiens (human) 2876 GPX1 inference by association of genotype from phenotype used in manual assertion
  • PMID:27077777
DOID:0070004 myeloid neoplasm HGNC:3498 Homo sapiens (human) 2122 MECOM inference by association of genotype from phenotype used in manual assertion
  • PMID:9044825
DOID:8683 myeloid sarcoma HGNC:6407 Homo sapiens (human) 3845 KRAS mutant phenotype evidence used in manual assertion
  • PMID:23564351
DOID:8683 myeloid sarcoma HGNC:8803 Homo sapiens (human) 5156 PDGFRA mutant phenotype evidence used in manual assertion
  • PMID:22348015
DOID:0060326 myelomeningocele HGNC:11005 Homo sapiens (human) 6513 SLC2A1 inference by association of genotype from phenotype used in manual assertion
  • PMID:21135204
  • PMID:23427181
DOID:0111344 myeloproliferative disorder with eosinophilia HGNC:8804 Homo sapiens (human) 5159 PDGFRB inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:2226 myeloproliferative neoplasm HGNC:25941 Homo sapiens (human) 54790 TET2 inference by association of genotype from phenotype used in manual assertion
  • PMID:19564637
DOID:2226 myeloproliferative neoplasm MGI:2684063 Mus musculus (house mouse) 228790 Asxl1 author statement supported by traceable reference
  • PMID:29113963
DOID:2226 myeloproliferative neoplasm MGI:97531 Mus musculus (house mouse) 18596 Pdgfrb author statement supported by traceable reference
  • MGI:5284969
DOID:2226 myeloproliferative neoplasm HGNC:8804 Homo sapiens (human) 5159 PDGFRB inference by association of genotype from phenotype used in manual assertion
  • PMID:12181402
DOID:5844 myocardial infarction HGNC:336 Homo sapiens (human) 185 AGTR1 inference by association of genotype from phenotype used in manual assertion
  • PMID:16061119
DOID:5844 myocardial infarction HGNC:7176 Homo sapiens (human) 4318 MMP9 inference by association of genotype from phenotype used in manual assertion
  • PMID:17893005
DOID:5844 myocardial infarction HGNC:587 Homo sapiens (human) 328 APEX1 inference by association of genotype from phenotype used in manual assertion
  • PMID:18712175
DOID:5844 myocardial infarction RGD:621007 Rattus norvegicus (Norway rat) 79128 Dab2 mutant phenotype evidence used in manual assertion
  • PMID:20666606
DOID:5844 myocardial infarction HGNC:4886 Homo sapiens (human) 3077 HFE inference by association of genotype from phenotype used in manual assertion
  • PMID:10491370
DOID:5844 myocardial infarction RGD:621065 Rattus norvegicus (Norway rat) 116630 Csf2 mutant phenotype evidence used in manual assertion
  • PMID:21326109
DOID:5844 myocardial infarction HGNC:9052 Homo sapiens (human) 5328 PLAU mutant phenotype evidence used in manual assertion
  • PMID:17653104
DOID:5844 myocardial infarction HGNC:3542 Homo sapiens (human) 2153 F5 inference by association of genotype from phenotype used in manual assertion
  • PMID:15131548
DOID:5844 myocardial infarction HGNC:7173 Homo sapiens (human) 4314 MMP3 inference by association of genotype from phenotype used in manual assertion
  • PMID:15467919
DOID:5844 myocardial infarction HGNC:613 Homo sapiens (human) 348 APOE inference by association of genotype from phenotype used in manual assertion
  • PMID:10090925
  • PMID:17217375
DOID:5844 myocardial infarction RGD:619894 Rattus norvegicus (Norway rat) 64672 Pln direct assay evidence used in manual assertion
  • PMID:23781262
DOID:5844 myocardial infarction RGD:69062 Rattus norvegicus (Norway rat) 83571 Cdkn1b mutant phenotype evidence used in manual assertion
  • PMID:22492676
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Supported by JST NBDC Grant Number JPMJND2204

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Last updated: April 7, 2025