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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 13801 - 13825 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence ▲ References
DOID:234 colon adenocarcinoma HGNC:16806 Homo sapiens (human) 51366 UBR5 mutant phenotype evidence used in manual assertion
  • PMID:28856538
  • PMID:29296225
DOID:9655 oral mucosa leukoplakia RGD:3889 Rattus norvegicus (Norway rat) 24842 Tp53 mutant phenotype evidence used in manual assertion
  • PMID:12167434
DOID:1184 nephrotic syndrome WB:WBGene00006365 Caenorhabditis elegans 180555 syg-1 mutant phenotype evidence used in manual assertion
  • PMID:20233749
DOID:8577 ulcerative colitis RGD:620349 Rattus norvegicus (Norway rat) 29527 Ptgs2 mutant phenotype evidence used in manual assertion
  • PMID:17429720
DOID:3234 central nervous system lymphoma HGNC:1133 Homo sapiens (human) 695 BTK mutant phenotype evidence used in manual assertion
  • PMID:28552327
DOID:5844 myocardial infarction HGNC:14388 Homo sapiens (human) 51206 GP6 mutant phenotype evidence used in manual assertion
  • PMID:22814400
DOID:4552 large cell carcinoma HGNC:9393 Homo sapiens (human) 5578 PRKCA mutant phenotype evidence used in manual assertion
  • PMID:9474241
DOID:10763 hypertension HGNC:1100 Homo sapiens (human) 672 BRCA1 mutant phenotype evidence used in manual assertion
  • PMID:24239235
DOID:3717 gastric adenocarcinoma HGNC:7133 Homo sapiens (human) 8085 KMT2D mutant phenotype evidence used in manual assertion
  • PMID:30177394
DOID:9970 obesity RGD:3234 Rattus norvegicus (Norway rat) 25601 Oprm1 mutant phenotype evidence used in manual assertion
  • PMID:16876155
DOID:3908 lung non-small cell carcinoma HGNC:3113 Homo sapiens (human) 1869 E2F1 mutant phenotype evidence used in manual assertion
  • PMID:12358350
DOID:5434 scrapie RGD:3410 Rattus norvegicus (Norway rat) 24686 Prnp mutant phenotype evidence used in manual assertion
  • PMID:29157304
DOID:2773 contact dermatitis HGNC:6953 Homo sapiens (human) 4179 CD46 mutant phenotype evidence used in manual assertion
  • PMID:12055630
DOID:169 neuroendocrine tumor HGNC:1455 Homo sapiens (human) 811 CALR mutant phenotype evidence used in manual assertion
  • PMID:16293970
DOID:4989 pancreatitis RGD:2201 Rattus norvegicus (Norway rat) 25245 Bdkrb2 mutant phenotype evidence used in manual assertion
  • PMID:7791078
DOID:6432 pulmonary hypertension HGNC:3179 Homo sapiens (human) 1909 EDNRA mutant phenotype evidence used in manual assertion
  • PMID:18506008
DOID:4362 cervical cancer HGNC:20815 Homo sapiens (human) 55818 KDM3A mutant phenotype evidence used in manual assertion
  • PMID:23492365
DOID:848 arthritis RGD:619713 Rattus norvegicus (Norway rat) 57302 Cnr2 mutant phenotype evidence used in manual assertion
  • PMID:18075852
DOID:0050589 inflammatory bowel disease HGNC:6000 Homo sapiens (human) 3557 IL1RN mutant phenotype evidence used in manual assertion
  • PMID:12184521
DOID:10283 prostate cancer HGNC:592 Homo sapiens (human) 331 XIAP mutant phenotype evidence used in manual assertion
  • PMID:19415464
DOID:9119 acute myeloid leukemia HGNC:6150 Homo sapiens (human) 3685 ITGAV mutant phenotype evidence used in manual assertion
  • PMID:23770013
DOID:10652 Alzheimer's disease RGD:620596 Rattus norvegicus (Norway rat) 117029 Ccr5 mutant phenotype evidence used in manual assertion
  • PMID:15979806
DOID:6039 uveal melanoma HGNC:8583 Homo sapiens (human) 5054 SERPINE1 mutant phenotype evidence used in manual assertion
  • PMID:9326241
DOID:4947 cholangiocarcinoma HGNC:11063 Homo sapiens (human) 8140 SLC7A5 mutant phenotype evidence used in manual assertion
  • PMID:24131658
  • PMID:28347255
DOID:0050861 colorectal adenocarcinoma HGNC:6307 Homo sapiens (human) 3791 KDR mutant phenotype evidence used in manual assertion
  • PMID:26325365
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Last updated: December 8, 2025