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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 14026 - 14050 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence ▲ References
DOID:7148 rheumatoid arthritis HGNC:11892 Homo sapiens (human) 7124 TNF mutant phenotype evidence used in manual assertion
  • PMID:12563673
DOID:9744 type 1 diabetes mellitus HGNC:5977 Homo sapiens (human) 3600 IL15 mutant phenotype evidence used in manual assertion
  • PMID:17670937
DOID:9352 type 2 diabetes mellitus HGNC:18124 Homo sapiens (human) 64805 P2RY12 mutant phenotype evidence used in manual assertion
  • PMID:15483100
DOID:769 neuroblastoma HGNC:5465 Homo sapiens (human) 3480 IGF1R mutant phenotype evidence used in manual assertion
  • PMID:17121898
DOID:12858 Huntington's disease HGNC:7866 Homo sapiens (human) 9241 NOG mutant phenotype evidence used in manual assertion
  • PMID:17885687
DOID:10941 intracranial aneurysm RGD:3645 Rattus norvegicus (Norway rat) 24770 Ccl2 mutant phenotype evidence used in manual assertion
  • PMID:19164781
DOID:3083 chronic obstructive pulmonary disease HGNC:3538 Homo sapiens (human) 2150 F2RL1 mutant phenotype evidence used in manual assertion
  • PMID:21245013
DOID:13250 diarrhea RGD:3098 Rattus norvegicus (Norway rat) 24590 Mme mutant phenotype evidence used in manual assertion
  • PMID:3481337
DOID:3571 liver cancer HGNC:1974 Homo sapiens (human) 1147 CHUK mutant phenotype evidence used in manual assertion
  • PMID:27367027
DOID:8536 herpes zoster HGNC:3535 Homo sapiens (human) 2147 F2 mutant phenotype evidence used in manual assertion
  • PMID:11449671
DOID:0050742 nicotine dependence RGD:61800 Rattus norvegicus (Norway rat) 29595 Htr2a mutant phenotype evidence used in manual assertion
  • PMID:22342986
DOID:3021 acute kidney failure RGD:628641 Rattus norvegicus (Norway rat) 84023 Ptger4 mutant phenotype evidence used in manual assertion
  • PMID:16871242
DOID:10952 nephritis RGD:2906 Rattus norvegicus (Norway rat) 29385 Cxcr2 mutant phenotype evidence used in manual assertion
  • PMID:11313419
DOID:13139 crescentic glomerulonephritis RGD:3645 Rattus norvegicus (Norway rat) 24770 Ccl2 mutant phenotype evidence used in manual assertion
  • PMID:8903512
DOID:684 hepatocellular carcinoma HGNC:20456 Homo sapiens (human) 84231 TRAF7 mutant phenotype evidence used in manual assertion
  • PMID:31730901
DOID:224 transient cerebral ischemia RGD:620598 Rattus norvegicus (Norway rat) 114243 Nox1 mutant phenotype evidence used in manual assertion
  • PMID:25617620
DOID:10908 hydrocephalus RGD:619777 Rattus norvegicus (Norway rat) 50687 L1cam mutant phenotype evidence used in manual assertion
  • PMID:30738385
DOID:6000 congestive heart failure RGD:1565646 Rattus norvegicus (Norway rat) 499593 Sox2 mutant phenotype evidence used in manual assertion
  • PMID:34321385
DOID:14330 Parkinson's disease WB:WBGene00002048 Caenorhabditis elegans 175807 ida-1 mutant phenotype evidence used in manual assertion
  • PMID:25469508
DOID:1324 lung cancer HGNC:30635 Homo sapiens (human) 11063 SOX30 mutant phenotype evidence used in manual assertion
  • PMID:25435374
DOID:4989 pancreatitis RGD:3371 Rattus norvegicus (Norway rat) 25664 Pparg mutant phenotype evidence used in manual assertion
  • PMID:18583255
DOID:9255 frontotemporal dementia HGNC:6893 Homo sapiens (human) 4137 MAPT mutant phenotype evidence used in manual assertion
  • PMID:16407562
DOID:10286 prostate carcinoma HGNC:9393 Homo sapiens (human) 5578 PRKCA mutant phenotype evidence used in manual assertion
  • PMID:9474241
DOID:0060108 brain glioma HGNC:9665 Homo sapiens (human) 5787 PTPRB mutant phenotype evidence used in manual assertion
  • PMID:16923162
DOID:1826 epilepsy RGD:628742 Rattus norvegicus (Norway rat) 252892 Lgi1 mutant phenotype evidence used in manual assertion
  • PMID:22589250
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Supported by JST NBDC Grant Number JPMJND2204

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Last updated: December 8, 2025