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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 13651 - 13675 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence ▲ References
DOID:162 cancer SGD:S000005816 Saccharomyces cerevisiae S288C 854465 SNF2 mutant phenotype evidence used in manual assertion
  • PMID:30700905
DOID:1596 depressive disorder HGNC:1963 Homo sapiens (human) 1142 CHRNB3 mutant phenotype evidence used in manual assertion
  • PMID:28420875
DOID:3910 lung adenocarcinoma HGNC:1455 Homo sapiens (human) 811 CALR mutant phenotype evidence used in manual assertion
  • PMID:18245558
DOID:3908 lung non-small cell carcinoma HGNC:12825 Homo sapiens (human) 7514 XPO1 mutant phenotype evidence used in manual assertion
  • PMID:24946002
  • PMID:31113936
DOID:2962 Cockayne syndrome WB:WBGene00008403 Caenorhabditis elegans 174474 csa-1 mutant phenotype evidence used in manual assertion
  • PMID:25453470
DOID:303 substance-related disorder RGD:619745 Rattus norvegicus (Norway rat) 192248 Cdh13 mutant phenotype evidence used in manual assertion
  • PMID:28387990
DOID:9281 phenylketonuria WB:WBGene00000253 Caenorhabditis elegans 171608 bli-3 mutant phenotype evidence used in manual assertion
  • PMID:18460651
DOID:9119 acute myeloid leukemia HGNC:2561 Homo sapiens (human) 7852 CXCR4 mutant phenotype evidence used in manual assertion
  • PMID:26031918
DOID:8683 myeloid sarcoma HGNC:6407 Homo sapiens (human) 3845 KRAS mutant phenotype evidence used in manual assertion
  • PMID:23564351
DOID:11132 prostatic hypertrophy HGNC:8800 Homo sapiens (human) 5155 PDGFB mutant phenotype evidence used in manual assertion
  • PMID:22689130
DOID:3910 lung adenocarcinoma HGNC:18420 Homo sapiens (human) 29072 SETD2 mutant phenotype evidence used in manual assertion
  • PMID:33223508
  • PMID:33707235
DOID:9675 pulmonary emphysema RGD:620349 Rattus norvegicus (Norway rat) 29527 Ptgs2 mutant phenotype evidence used in manual assertion
  • PMID:20472710
DOID:3498 pancreatic ductal adenocarcinoma HGNC:11772 Homo sapiens (human) 7046 TGFBR1 mutant phenotype evidence used in manual assertion
  • PMID:17297450
DOID:332 amyotrophic lateral sclerosis WB:WBGene00006575 Caenorhabditis elegans 175502 tir-1 mutant phenotype evidence used in manual assertion
  • PMID:26059317
DOID:4362 cervical cancer HGNC:6846 Homo sapiens (human) 5608 MAP2K6 mutant phenotype evidence used in manual assertion
  • PMID:20980434
DOID:0111223 centronuclear myopathy 1 SGD:S000001709 Saccharomyces cerevisiae S288C 853870 VPS1 mutant phenotype evidence used in manual assertion
  • PMID:28357347
  • PMID:37060997
DOID:6000 congestive heart failure RGD:2070 Rattus norvegicus (Norway rat) 24180 Agtr1a mutant phenotype evidence used in manual assertion
  • PMID:21963897
DOID:431 myofascial pain syndrome RGD:620144 Rattus norvegicus (Norway rat) 59109 Ntrk1 mutant phenotype evidence used in manual assertion
  • PMID:21719352
DOID:11394 adult respiratory distress syndrome HGNC:11917 Homo sapiens (human) 7133 TNFRSF1B mutant phenotype evidence used in manual assertion
  • PMID:19916860
DOID:1793 pancreatic cancer HGNC:7514 Homo sapiens (human) 4585 MUC4 mutant phenotype evidence used in manual assertion
  • PMID:17406026
  • PMID:17595659
DOID:1793 pancreatic cancer HGNC:6470 Homo sapiens (human) 3897 L1CAM mutant phenotype evidence used in manual assertion
  • PMID:22095073
DOID:10652 Alzheimer's disease HGNC:620 Homo sapiens (human) 351 APP mutant phenotype evidence used in manual assertion
  • PMID:11520987
  • PMID:17506994
  • PMID:29641600
DOID:2316 brain ischemia RGD:3186 Rattus norvegicus (Norway rat) 24600 Nos3 mutant phenotype evidence used in manual assertion
  • PMID:17600658
DOID:3021 acute kidney failure RGD:2493 Rattus norvegicus (Norway rat) 24310 Ace mutant phenotype evidence used in manual assertion
  • PMID:24502693
DOID:9538 multiple myeloma HGNC:10249 Homo sapiens (human) 6091 ROBO1 mutant phenotype evidence used in manual assertion
  • PMID:34268498
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Last updated: December 8, 2025