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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 13476 - 13500 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence ▲ References
DOID:3910 lung adenocarcinoma HGNC:1919 Homo sapiens (human) 1108 CHD4 mutant phenotype evidence used in manual assertion
  • PMID:32228507
DOID:10763 hypertension HGNC:2634 Homo sapiens (human) 1573 CYP2J2 mutant phenotype evidence used in manual assertion
  • PMID:20501636
DOID:2384 Wernicke encephalopathy RGD:620349 Rattus norvegicus (Norway rat) 29527 Ptgs2 mutant phenotype evidence used in manual assertion
  • PMID:18481165
DOID:784 chronic kidney disease RGD:2070 Rattus norvegicus (Norway rat) 24180 Agtr1a mutant phenotype evidence used in manual assertion
  • PMID:12089373
DOID:3347 osteosarcoma RGD:3889 Rattus norvegicus (Norway rat) 24842 Tp53 mutant phenotype evidence used in manual assertion
  • PMID:27528400
DOID:6432 pulmonary hypertension RGD:619796 Rattus norvegicus (Norway rat) 114099 Cysltr1 mutant phenotype evidence used in manual assertion
  • PMID:12910720
DOID:0080855 Parkinsonism RGD:2369 Rattus norvegicus (Norway rat) 25248 Cnr1 mutant phenotype evidence used in manual assertion
  • PMID:19414037
DOID:0060071 pre-malignant neoplasm RGD:2493 Rattus norvegicus (Norway rat) 24310 Ace mutant phenotype evidence used in manual assertion
  • PMID:24959250
DOID:0050745 diffuse large B-cell lymphoma HGNC:1699 Homo sapiens (human) 974 CD79B mutant phenotype evidence used in manual assertion
  • PMID:25708834
DOID:5082 liver cirrhosis HGNC:8941 Homo sapiens (human) 5265 SERPINA1 mutant phenotype evidence used in manual assertion
  • PMID:20522742
DOID:10652 Alzheimer's disease HGNC:7154 Homo sapiens (human) 4311 MME mutant phenotype evidence used in manual assertion
  • PMID:25884928
DOID:9256 colorectal cancer HGNC:3236 Homo sapiens (human) 1956 EGFR mutant phenotype evidence used in manual assertion
  • PMID:15269313
  • PMID:21398618
DOID:0060060 non-Hodgkin lymphoma HGNC:1699 Homo sapiens (human) 974 CD79B mutant phenotype evidence used in manual assertion
  • PMID:19633198
DOID:8692 myeloid leukemia HGNC:3688 Homo sapiens (human) 2260 FGFR1 mutant phenotype evidence used in manual assertion
  • PMID:19506298
DOID:6000 congestive heart failure RGD:2059 Rattus norvegicus (Norway rat) 24925 Adrb1 mutant phenotype evidence used in manual assertion
  • PMID:19587314
DOID:4362 cervical cancer HGNC:18541 Homo sapiens (human) 55904 KMT2E mutant phenotype evidence used in manual assertion
  • PMID:25172963
DOID:231 motor neuron disease HGNC:11179 Homo sapiens (human) 6647 SOD1 mutant phenotype evidence used in manual assertion
  • PMID:11717358
DOID:4195 hyperglycemia HGNC:6107 Homo sapiens (human) 3651 PDX1 mutant phenotype evidence used in manual assertion
  • PMID:17131142
DOID:12241 beta thalassemia HGNC:4827 Homo sapiens (human) 3043 HBB mutant phenotype evidence used in manual assertion
  • PMID:16631345
DOID:5176 renal Wilms' tumor HGNC:8616 Homo sapiens (human) 5076 PAX2 mutant phenotype evidence used in manual assertion
  • PMID:18467665
DOID:0050741 alcohol dependence HGNC:8156 Homo sapiens (human) 4988 OPRM1 mutant phenotype evidence used in manual assertion
  • PMID:30748046
DOID:3770 pulmonary fibrosis RGD:3249 Rattus norvegicus (Norway rat) 24617 Serpine1 mutant phenotype evidence used in manual assertion
  • PMID:22659625
DOID:0050741 alcohol dependence RGD:2677 Rattus norvegicus (Norway rat) 25453 Gdnf mutant phenotype evidence used in manual assertion
  • PMID:15659598
  • PMID:24801661
DOID:9352 type 2 diabetes mellitus WB:WBGene00003858 Caenorhabditis elegans 176000 ogt-1 mutant phenotype evidence used in manual assertion
  • PMID:16051707
  • PMID:16882729
DOID:12361 Graves' disease HGNC:11935 Homo sapiens (human) 959 CD40LG mutant phenotype evidence used in manual assertion
  • PMID:8875745
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Supported by JST NBDC Grant Number JPMJND2204

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Last updated: December 8, 2025