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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 13276 - 13300 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence ▲ References
DOID:0060041 autism spectrum disorder RGD:621119 Rattus norvegicus (Norway rat) 171297 Nlgn3 mutant phenotype evidence used in manual assertion
  • PMID:24773431
  • PMID:28958035
DOID:11446 sciatic neuropathy RGD:2802 Rattus norvegicus (Norway rat) 25459 Hmgb1 mutant phenotype evidence used in manual assertion
  • PMID:23991202
DOID:332 amyotrophic lateral sclerosis RGD:70553 Rattus norvegicus (Norway rat) 113959 C5ar1 mutant phenotype evidence used in manual assertion
  • PMID:19050293
DOID:3070 high grade glioma SGD:S000004164 Saccharomyces cerevisiae S288C 850871 IDP2 mutant phenotype evidence used in manual assertion
  • PMID:27427385
DOID:219 colon cancer HGNC:11063 Homo sapiens (human) 8140 SLC7A5 mutant phenotype evidence used in manual assertion
  • PMID:19900191
DOID:10584 retinitis pigmentosa HGNC:11179 Homo sapiens (human) 6647 SOD1 mutant phenotype evidence used in manual assertion
  • PMID:19293779
DOID:3082 interstitial lung disease RGD:2890 Rattus norvegicus (Norway rat) 24493 Il1a mutant phenotype evidence used in manual assertion
  • PMID:1826836
DOID:5176 renal Wilms' tumor HGNC:11724 Homo sapiens (human) 7010 TEK mutant phenotype evidence used in manual assertion
  • PMID:18467665
DOID:2841 asthma RGD:3283 Rattus norvegicus (Norway rat) 24628 Pdgfb mutant phenotype evidence used in manual assertion
  • PMID:21216974
DOID:2841 asthma HGNC:1030 Homo sapiens (human) 624 BDKRB2 mutant phenotype evidence used in manual assertion
  • PMID:8856156
DOID:0080202 adenoid cystic carcinoma HGNC:8033 Homo sapiens (human) 4916 NTRK3 mutant phenotype evidence used in manual assertion
  • PMID:23027130
DOID:3068 glioblastoma HGNC:9665 Homo sapiens (human) 5787 PTPRB mutant phenotype evidence used in manual assertion
  • PMID:16489031
DOID:3068 glioblastoma RGD:735225 Rattus norvegicus (Norway rat) 295703 Serping1 mutant phenotype evidence used in manual assertion
  • PMID:28880870
DOID:3082 interstitial lung disease RGD:3645 Rattus norvegicus (Norway rat) 24770 Ccl2 mutant phenotype evidence used in manual assertion
  • PMID:1387671
DOID:289 endometriosis HGNC:11917 Homo sapiens (human) 7133 TNFRSF1B mutant phenotype evidence used in manual assertion
  • PMID:21481092
DOID:1824 status epilepticus RGD:620458 Rattus norvegicus (Norway rat) 89808 Cx3cl1 mutant phenotype evidence used in manual assertion
  • PMID:21481949
DOID:13372 alpha 1-antitrypsin deficiency HGNC:8941 Homo sapiens (human) 5265 SERPINA1 mutant phenotype evidence used in manual assertion
  • PMID:29641323
DOID:3068 glioblastoma HGNC:3527 Homo sapiens (human) 2146 EZH2 mutant phenotype evidence used in manual assertion
  • PMID:25595591
DOID:1287 cardiovascular system disease HGNC:9605 Homo sapiens (human) 5743 PTGS2 mutant phenotype evidence used in manual assertion
  • PMID:21843325
DOID:1793 pancreatic cancer HGNC:3236 Homo sapiens (human) 1956 EGFR mutant phenotype evidence used in manual assertion
  • PMID:17452677
DOID:9452 steatotic liver disease RGD:2998 Rattus norvegicus (Norway rat) 300438 Ldlr mutant phenotype evidence used in manual assertion
  • PMID:29459263
DOID:10247 pleurisy RGD:3644 Rattus norvegicus (Norway rat) 29397 Ccl11 mutant phenotype evidence used in manual assertion
  • PMID:11564646
DOID:0080855 Parkinsonism RGD:2379 Rattus norvegicus (Norway rat) 24267 Comt mutant phenotype evidence used in manual assertion
  • PMID:15698633
DOID:3908 lung non-small cell carcinoma HGNC:12637 Homo sapiens (human) 7403 KDM6A mutant phenotype evidence used in manual assertion
  • PMID:32879445
DOID:684 hepatocellular carcinoma HGNC:5173 Homo sapiens (human) 3265 HRAS mutant phenotype evidence used in manual assertion
  • PMID:10791191
  • PMID:23555816
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Supported by JST NBDC Grant Number JPMJND2204

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Last updated: December 8, 2025