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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 13576 - 13600 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence ▲ References
DOID:4947 cholangiocarcinoma HGNC:9253 Homo sapiens (human) 5478 PPIA mutant phenotype evidence used in manual assertion
  • PMID:21871105
DOID:1793 pancreatic cancer HGNC:10717 Homo sapiens (human) 6400 SEL1L mutant phenotype evidence used in manual assertion
  • PMID:14508516
DOID:4467 clear cell renal cell carcinoma HGNC:5465 Homo sapiens (human) 3480 IGF1R mutant phenotype evidence used in manual assertion
  • PMID:19509240
DOID:0081292 traumatic brain injury RGD:3889 Rattus norvegicus (Norway rat) 24842 Tp53 mutant phenotype evidence used in manual assertion
  • PMID:27553877
DOID:4450 renal cell carcinoma HGNC:11892 Homo sapiens (human) 7124 TNF mutant phenotype evidence used in manual assertion
  • PMID:19384924
DOID:7188 autoimmune thyroiditis HGNC:4948 Homo sapiens (human) 3123 HLA-DRB1 mutant phenotype evidence used in manual assertion
  • PMID:21683551
DOID:1184 nephrotic syndrome RGD:620349 Rattus norvegicus (Norway rat) 29527 Ptgs2 mutant phenotype evidence used in manual assertion
  • PMID:19194550
DOID:0060903 thrombosis RGD:70553 Rattus norvegicus (Norway rat) 113959 C5ar1 mutant phenotype evidence used in manual assertion
  • PMID:11422211
DOID:4989 pancreatitis RGD:3811 Rattus norvegicus (Norway rat) 24807 Tacr1 mutant phenotype evidence used in manual assertion
  • PMID:18580444
DOID:12858 Huntington's disease HGNC:6018 Homo sapiens (human) 3569 IL6 mutant phenotype evidence used in manual assertion
  • PMID:11860469
DOID:9993 hypoglycemia HGNC:12519 Homo sapiens (human) 7352 UCP3 mutant phenotype evidence used in manual assertion
  • PMID:10935638
DOID:3021 acute kidney failure RGD:2185 Rattus norvegicus (Norway rat) 25107 Avpr1a mutant phenotype evidence used in manual assertion
  • PMID:17347933
DOID:0080599 Coronavirus infectious disease HGNC:2707 Homo sapiens (human) 1636 ACE mutant phenotype evidence used in manual assertion
  • PMID:17108019
DOID:9884 muscular dystrophy WB:WBGene00002248 Caenorhabditis elegans 172952 lam-3 mutant phenotype evidence used in manual assertion
  • PMID:12783803
DOID:3908 lung non-small cell carcinoma HGNC:9955 Homo sapiens (human) 5970 RELA mutant phenotype evidence used in manual assertion
  • PMID:16287968
DOID:0080855 Parkinsonism RGD:621647 Rattus norvegicus (Norway rat) 117064 Vip mutant phenotype evidence used in manual assertion
  • PMID:15808913
DOID:1380 endometrial cancer HGNC:3219 Homo sapiens (human) 30008 EFEMP2 mutant phenotype evidence used in manual assertion
  • PMID:28177909
DOID:0050200 Korean hemorrhagic fever RGD:2895 Rattus norvegicus (Norway rat) 25704 Il2ra mutant phenotype evidence used in manual assertion
  • PMID:17878294
DOID:0050431 arrhythmogenic right ventricular cardiomyopathy HGNC:3049 Homo sapiens (human) 1829 DSG2 mutant phenotype evidence used in manual assertion
  • PMID:30304392
DOID:5844 myocardial infarction HGNC:12681 Homo sapiens (human) 7423 VEGFB mutant phenotype evidence used in manual assertion
  • PMID:17975666
DOID:2526 prostate adenocarcinoma HGNC:391 Homo sapiens (human) 207 AKT1 mutant phenotype evidence used in manual assertion
  • PMID:20638364
DOID:4906 small intestine adenocarcinoma HGNC:6842 Homo sapiens (human) 5605 MAP2K2 mutant phenotype evidence used in manual assertion
  • PMID:19014680
DOID:824 periodontitis RGD:2059 Rattus norvegicus (Norway rat) 24925 Adrb1 mutant phenotype evidence used in manual assertion
  • PMID:18275933
DOID:684 hepatocellular carcinoma HGNC:25941 Homo sapiens (human) 54790 TET2 mutant phenotype evidence used in manual assertion
  • PMID:29331390
  • PMID:33097695
DOID:8947 diabetic retinopathy RGD:2143 Rattus norvegicus (Norway rat) 25293 Aqp4 mutant phenotype evidence used in manual assertion
  • PMID:22449442
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Supported by JST NBDC Grant Number JPMJND2204

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Last updated: December 8, 2025