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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 12901 - 12925 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence ▲ References
DOID:0050855 renal fibrosis HGNC:7155 Homo sapiens (human) 4312 MMP1 mutant phenotype evidence used in manual assertion
  • PMID:14674437
DOID:13619 extrahepatic cholestasis RGD:3285 Rattus norvegicus (Norway rat) 24629 Pdgfrb mutant phenotype evidence used in manual assertion
  • PMID:18466260
DOID:10763 hypertension RGD:620401 Rattus norvegicus (Norway rat) 81509 Bdkrb1 mutant phenotype evidence used in manual assertion
  • PMID:17988733
DOID:1612 breast cancer HGNC:1785 Homo sapiens (human) 1027 CDKN1B mutant phenotype evidence used in manual assertion
  • PMID:18030569
DOID:1574 alcohol use disorder WB:WBGene00001172 Caenorhabditis elegans 179412 egl-3 mutant phenotype evidence used in manual assertion
  • PMID:19535903
DOID:10652 Alzheimer's disease HGNC:4948 Homo sapiens (human) 3123 HLA-DRB1 mutant phenotype evidence used in manual assertion
  • PMID:21473952
DOID:12932 endomyocardial fibrosis RGD:621884 Rattus norvegicus (Norway rat) 57305 Uts2r mutant phenotype evidence used in manual assertion
  • PMID:16919371
DOID:13580 cholestasis RGD:2990 Rattus norvegicus (Norway rat) 24944 Lamp2 mutant phenotype evidence used in manual assertion
  • PMID:28124283
DOID:2841 asthma HGNC:10623 Homo sapiens (human) 6369 CCL24 mutant phenotype evidence used in manual assertion
  • PMID:17548626
DOID:1793 pancreatic cancer HGNC:9605 Homo sapiens (human) 5743 PTGS2 mutant phenotype evidence used in manual assertion
  • PMID:20216081
DOID:7148 rheumatoid arthritis HGNC:11920 Homo sapiens (human) 355 FAS mutant phenotype evidence used in manual assertion
  • PMID:20875116
DOID:684 hepatocellular carcinoma HGNC:18505 Homo sapiens (human) 54894 RNF43 mutant phenotype evidence used in manual assertion
  • PMID:23136185
DOID:9743 diabetic neuropathy HGNC:4893 Homo sapiens (human) 3082 HGF mutant phenotype evidence used in manual assertion
  • PMID:15734864
DOID:10247 pleurisy RGD:620401 Rattus norvegicus (Norway rat) 81509 Bdkrb1 mutant phenotype evidence used in manual assertion
  • PMID:11853231
DOID:224 transient cerebral ischemia RGD:3371 Rattus norvegicus (Norway rat) 25664 Pparg mutant phenotype evidence used in manual assertion
  • PMID:18378216
  • PMID:19221220
DOID:2921 glomerulonephritis RGD:3752 Rattus norvegicus (Norway rat) 25353 Spp1 mutant phenotype evidence used in manual assertion
  • PMID:20720406
DOID:813 septic arthritis RGD:2306 Rattus norvegicus (Norway rat) 24932 Cd4 mutant phenotype evidence used in manual assertion
  • PMID:1730259
DOID:9119 acute myeloid leukemia SGD:S000003060 Saccharomyces cerevisiae S288C 852788 NUP145 mutant phenotype evidence used in manual assertion
  • PMID:29034209
DOID:224 transient cerebral ischemia RGD:2582 Rattus norvegicus (Norway rat) 25149 Esr2 mutant phenotype evidence used in manual assertion
  • PMID:23593292
DOID:10534 stomach cancer HGNC:11110 Homo sapiens (human) 8289 ARID1A mutant phenotype evidence used in manual assertion
  • PMID:27323812
DOID:8869 neuromyelitis optica RGD:2311 Rattus norvegicus (Norway rat) 25407 Cd59b mutant phenotype evidence used in manual assertion
  • PMID:28212662
DOID:8534 gastroesophageal reflux disease HGNC:9031 Homo sapiens (human) 5320 PLA2G2A mutant phenotype evidence used in manual assertion
  • PMID:19672667
DOID:3571 liver cancer HGNC:5960 Homo sapiens (human) 3551 IKBKB mutant phenotype evidence used in manual assertion
  • PMID:27367027
DOID:8566 herpes simplex HGNC:613 Homo sapiens (human) 348 APOE mutant phenotype evidence used in manual assertion
  • PMID:17101197
DOID:234 colon adenocarcinoma HGNC:11283 Homo sapiens (human) 6714 SRC mutant phenotype evidence used in manual assertion
  • PMID:21282564
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Last updated: December 8, 2025