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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 13101 - 13125 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence ▲ References
DOID:3803 Crigler-Najjar syndrome RGD:3935 Rattus norvegicus (Norway rat) 24861 Ugt1a1 mutant phenotype evidence used in manual assertion
  • PMID:22765254
DOID:0110184 Charcot-Marie-Tooth disease type 4J SGD:S000005269 Saccharomyces cerevisiae S288C 855392 FIG4 mutant phenotype evidence used in manual assertion
  • PMID:17572665
DOID:5844 myocardial infarction RGD:2059 Rattus norvegicus (Norway rat) 24925 Adrb1 mutant phenotype evidence used in manual assertion
  • PMID:17143192
DOID:684 hepatocellular carcinoma HGNC:3688 Homo sapiens (human) 2260 FGFR1 mutant phenotype evidence used in manual assertion
  • PMID:21573021
DOID:0060574 von Willebrand's disease 2 HGNC:12726 Homo sapiens (human) 7450 VWF mutant phenotype evidence used in manual assertion
  • PMID:20589313
DOID:0080599 Coronavirus infectious disease HGNC:1641 Homo sapiens (human) 30835 CD209 mutant phenotype evidence used in manual assertion
  • PMID:20864747
DOID:14330 Parkinson's disease HGNC:3415 Homo sapiens (human) 2056 EPO mutant phenotype evidence used in manual assertion
  • PMID:19727138
DOID:3525 middle cerebral artery infarction RGD:67378 Rattus norvegicus (Norway rat) 24586 Ncam1 mutant phenotype evidence used in manual assertion
  • PMID:29497380
DOID:2355 anemia HGNC:2707 Homo sapiens (human) 1636 ACE mutant phenotype evidence used in manual assertion
  • PMID:23141116
DOID:1324 lung cancer HGNC:1455 Homo sapiens (human) 811 CALR mutant phenotype evidence used in manual assertion
  • PMID:12215887
DOID:684 hepatocellular carcinoma HGNC:11621 Homo sapiens (human) 6927 HNF1A mutant phenotype evidence used in manual assertion
  • PMID:29466992
DOID:2316 brain ischemia HGNC:8893 Homo sapiens (human) 5228 PGF mutant phenotype evidence used in manual assertion
  • PMID:16901914
DOID:10652 Alzheimer's disease WB:WBGene00003001 Caenorhabditis elegans 176282 lin-12 mutant phenotype evidence used in manual assertion
  • PMID:7566091
DOID:2340 craniosynostosis HGNC:3689 Homo sapiens (human) 2263 FGFR2 mutant phenotype evidence used in manual assertion
  • PMID:19627528
DOID:1936 atherosclerosis HGNC:13633 Homo sapiens (human) 9370 ADIPOQ mutant phenotype evidence used in manual assertion
  • PMID:12451000
DOID:263 kidney cancer HGNC:3687 Homo sapiens (human) 2254 FGF9 mutant phenotype evidence used in manual assertion
  • PMID:26183774
DOID:9256 colorectal cancer HGNC:12637 Homo sapiens (human) 7403 KDM6A mutant phenotype evidence used in manual assertion
  • PMID:31139021
DOID:0110663 congenital myasthenic syndrome 1A HGNC:1515 Homo sapiens (human) 831 CAST mutant phenotype evidence used in manual assertion
  • PMID:17853947
DOID:437 myasthenia gravis HGNC:108 Homo sapiens (human) 43 ACHE mutant phenotype evidence used in manual assertion
  • PMID:17986328
DOID:3498 pancreatic ductal adenocarcinoma HGNC:4432 Homo sapiens (human) 2805 GOT1 mutant phenotype evidence used in manual assertion
  • PMID:23535601
DOID:6000 congestive heart failure RGD:2053 Rattus norvegicus (Norway rat) 25591 Parp1 mutant phenotype evidence used in manual assertion
  • PMID:19443425
DOID:10763 hypertension RGD:3329 Rattus norvegicus (Norway rat) 25513 Pik3r1 mutant phenotype evidence used in manual assertion
  • PMID:19015400
DOID:3525 middle cerebral artery infarction RGD:2143 Rattus norvegicus (Norway rat) 25293 Aqp4 mutant phenotype evidence used in manual assertion
  • PMID:33127515
DOID:2841 asthma HGNC:5006 Homo sapiens (human) 3156 HMGCR mutant phenotype evidence used in manual assertion
  • PMID:20084838
DOID:12930 dilated cardiomyopathy RGD:2059 Rattus norvegicus (Norway rat) 24925 Adrb1 mutant phenotype evidence used in manual assertion
  • PMID:18287209
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Supported by JST NBDC Grant Number JPMJND2204

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Last updated: December 8, 2025