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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 13926 - 13950 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence ▲ References
DOID:809 cocaine abuse RGD:2848 Rattus norvegicus (Norway rat) 25187 Htr2c mutant phenotype evidence used in manual assertion
  • PMID:20814782
DOID:0080199 colorectal carcinoma HGNC:3438 Homo sapiens (human) 2074 ERCC6 mutant phenotype evidence used in manual assertion
  • PMID:28665687
DOID:6432 pulmonary hypertension RGD:61997 Rattus norvegicus (Norway rat) 29553 Kcnk3 mutant phenotype evidence used in manual assertion
  • PMID:31347976
DOID:10534 stomach cancer HGNC:3214 Homo sapiens (human) 1938 EEF2 mutant phenotype evidence used in manual assertion
  • PMID:19360331
DOID:0050934 ovarian clear cell carcinoma HGNC:11110 Homo sapiens (human) 8289 ARID1A mutant phenotype evidence used in manual assertion
  • PMID:21900401
DOID:684 hepatocellular carcinoma HGNC:29608 Homo sapiens (human) 92140 MTDH mutant phenotype evidence used in manual assertion
  • PMID:26351209
DOID:1612 breast cancer HGNC:11364 Homo sapiens (human) 6774 STAT3 mutant phenotype evidence used in manual assertion
  • PMID:15374974
  • PMID:21740845
DOID:9119 acute myeloid leukemia HGNC:6018 Homo sapiens (human) 3569 IL6 mutant phenotype evidence used in manual assertion
  • PMID:8892684
DOID:684 hepatocellular carcinoma HGNC:10783 Homo sapiens (human) 6427 SRSF2 mutant phenotype evidence used in manual assertion
  • PMID:28082404
DOID:707 B-cell lymphoma HGNC:3527 Homo sapiens (human) 2146 EZH2 mutant phenotype evidence used in manual assertion
  • PMID:29456795
DOID:14330 Parkinson's disease SGD:S000005113 Saccharomyces cerevisiae S288C 855552 PSD1 mutant phenotype evidence used in manual assertion
  • PMID:25201965
DOID:6432 pulmonary hypertension RGD:621376 Rattus norvegicus (Norway rat) 94271 Atp5pf mutant phenotype evidence used in manual assertion
  • PMID:27491388
DOID:3910 lung adenocarcinoma HGNC:24308 Homo sapiens (human) 81037 CLPTM1L mutant phenotype evidence used in manual assertion
  • PMID:24366883
DOID:0060284 paroxysmal nocturnal hemoglobinuria SGD:S000006096 Saccharomyces cerevisiae S288C 855928 SPT14 mutant phenotype evidence used in manual assertion
  • PMID:7737116
DOID:162 cancer SGD:S000001542 Saccharomyces cerevisiae S288C 853806 MPE1 mutant phenotype evidence used in manual assertion
  • PMID:30700905
DOID:0050746 mantle cell lymphoma HGNC:1133 Homo sapiens (human) 695 BTK mutant phenotype evidence used in manual assertion
  • PMID:23045577
DOID:0050741 alcohol dependence RGD:3057 Rattus norvegicus (Norway rat) 25635 Mc4r mutant phenotype evidence used in manual assertion
  • PMID:24635847
DOID:83 cataract HGNC:381 Homo sapiens (human) 231 AKR1B1 mutant phenotype evidence used in manual assertion
  • PMID:21329682
DOID:13207 proliferative diabetic retinopathy HGNC:9236 Homo sapiens (human) 5468 PPARG mutant phenotype evidence used in manual assertion
  • PMID:18541841
DOID:5844 myocardial infarction RGD:621237 Rattus norvegicus (Norway rat) 25625 Tnfrsf1a mutant phenotype evidence used in manual assertion
  • PMID:20651834
DOID:2154 nephroblastoma HGNC:5465 Homo sapiens (human) 3480 IGF1R mutant phenotype evidence used in manual assertion
  • PMID:22529373
  • PMID:8390684
DOID:2234 focal epilepsy RGD:2369 Rattus norvegicus (Norway rat) 25248 Cnr1 mutant phenotype evidence used in manual assertion
  • PMID:19595742
DOID:5844 myocardial infarction RGD:69062 Rattus norvegicus (Norway rat) 83571 Cdkn1b mutant phenotype evidence used in manual assertion
  • PMID:22492676
DOID:11832 visual epilepsy RGD:3283 Rattus norvegicus (Norway rat) 24628 Pdgfb mutant phenotype evidence used in manual assertion
  • PMID:14980813
DOID:5082 liver cirrhosis RGD:619868 Rattus norvegicus (Norway rat) 25283 Gclc mutant phenotype evidence used in manual assertion
  • PMID:22942279
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Last updated: December 8, 2025