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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 14101 - 14125 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:1602 Homo sapiens (human) 1230 CCR1 mutant phenotype evidence used in manual assertion
  • PMID:12860725
DOID:4074 pancreatic adenocarcinoma HGNC:9801 Homo sapiens (human) 5879 RAC1 mutant phenotype evidence used in manual assertion
  • PMID:21037555
DOID:8893 psoriasis HGNC:5981 Homo sapiens (human) 3605 IL17A mutant phenotype evidence used in manual assertion
  • PMID:20926833
DOID:684 hepatocellular carcinoma HGNC:10771 Homo sapiens (human) 10262 SF3B4 mutant phenotype evidence used in manual assertion
  • PMID:30391496
DOID:10808 gastric ulcer RGD:620349 Rattus norvegicus (Norway rat) 29527 Ptgs2 mutant phenotype evidence used in manual assertion
  • PMID:17673547
DOID:9970 obesity WB:WBGene00001650 Caenorhabditis elegans 177850 gon-1 mutant phenotype evidence used in manual assertion
  • PMID:34492009
DOID:1686 glaucoma HGNC:3263 Homo sapiens (human) 27161 AGO2 mutant phenotype evidence used in manual assertion
  • PMID:29392316
DOID:3910 lung adenocarcinoma HGNC:3691 Homo sapiens (human) 2264 FGFR4 mutant phenotype evidence used in manual assertion
  • PMID:29402970
DOID:0080547 metabolic dysfunction-associated steatohepatitis HGNC:600 Homo sapiens (human) 335 APOA1 mutant phenotype evidence used in manual assertion
  • PMID:24793484
DOID:4450 renal cell carcinoma HGNC:9955 Homo sapiens (human) 5970 RELA mutant phenotype evidence used in manual assertion
  • PMID:17290398
DOID:4029 gastritis RGD:62084 Rattus norvegicus (Norway rat) 29319 Cblif mutant phenotype evidence used in manual assertion
  • PMID:1097299
DOID:9352 type 2 diabetes mellitus RGD:1308903 Rattus norvegicus (Norway rat) 310615 Crtc2 mutant phenotype evidence used in manual assertion
  • PMID:19706791
  • PMID:23595987
DOID:14323 Marfan syndrome WB:WBGene00000900 Caenorhabditis elegans 175781 daf-4 mutant phenotype evidence used in manual assertion
  • PMID:31071172
DOID:5844 myocardial infarction RGD:621065 Rattus norvegicus (Norway rat) 116630 Csf2 mutant phenotype evidence used in manual assertion
  • PMID:21326109
DOID:1793 pancreatic cancer HGNC:1571 Homo sapiens (human) 887 CCKBR mutant phenotype evidence used in manual assertion
  • PMID:15688412
DOID:820 myocarditis RGD:628641 Rattus norvegicus (Norway rat) 84023 Ptger4 mutant phenotype evidence used in manual assertion
  • PMID:21383594
DOID:13141 uveitis RGD:621237 Rattus norvegicus (Norway rat) 25625 Tnfrsf1a mutant phenotype evidence used in manual assertion
  • PMID:12824249
DOID:11394 adult respiratory distress syndrome RGD:3747 Rattus norvegicus (Norway rat) 24795 Serpina3n mutant phenotype evidence used in manual assertion
  • PMID:8574716
DOID:9743 diabetic neuropathy RGD:620349 Rattus norvegicus (Norway rat) 29527 Ptgs2 mutant phenotype evidence used in manual assertion
  • PMID:17720896
DOID:3070 high grade glioma RGD:2802 Rattus norvegicus (Norway rat) 25459 Hmgb1 mutant phenotype evidence used in manual assertion
  • PMID:10830965
DOID:8725 vascular dementia RGD:620598 Rattus norvegicus (Norway rat) 114243 Nox1 mutant phenotype evidence used in manual assertion
  • PMID:24294978
DOID:574 peripheral nervous system disease RGD:621427 Rattus norvegicus (Norway rat) 362572 Artn mutant phenotype evidence used in manual assertion
  • PMID:18344995
DOID:0080600 COVID-19 HGNC:18363 Homo sapiens (human) 282618 IFNL1 mutant phenotype evidence used in manual assertion
  • PMID:32854108
DOID:5425 ovarian hyperstimulation syndrome RGD:619991 Rattus norvegicus (Norway rat) 83785 Vegfa mutant phenotype evidence used in manual assertion
  • PMID:25151950
DOID:3070 high grade glioma RGD:2149 Rattus norvegicus (Norway rat) 29183 Areg mutant phenotype evidence used in manual assertion
  • PMID:8621257
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Last updated: December 8, 2025