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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 14051 - 14075 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence ▲ References
DOID:9351 diabetes mellitus HGNC:5006 Homo sapiens (human) 3156 HMGCR mutant phenotype evidence used in manual assertion
  • PMID:15476492
DOID:649 prion disease HGNC:11179 Homo sapiens (human) 6647 SOD1 mutant phenotype evidence used in manual assertion
  • PMID:18559949
DOID:9256 colorectal cancer HGNC:12825 Homo sapiens (human) 7514 XPO1 mutant phenotype evidence used in manual assertion
  • PMID:26603256
  • PMID:33745946
DOID:10763 hypertension RGD:2072 Rattus norvegicus (Norway rat) 24182 Agtr2 mutant phenotype evidence used in manual assertion
  • PMID:19680135
  • PMID:21040717
DOID:9352 type 2 diabetes mellitus HGNC:9291 Homo sapiens (human) 5506 PPP1R3A mutant phenotype evidence used in manual assertion
  • PMID:11793847
DOID:2841 asthma HGNC:6000 Homo sapiens (human) 3557 IL1RN mutant phenotype evidence used in manual assertion
  • PMID:16724092
DOID:13141 uveitis HGNC:11892 Homo sapiens (human) 7124 TNF mutant phenotype evidence used in manual assertion
  • PMID:20673052
DOID:14323 Marfan syndrome WB:WBGene00003482 Caenorhabditis elegans 176430 mua-3 mutant phenotype evidence used in manual assertion
  • PMID:25917920
DOID:2841 asthma HGNC:435 Homo sapiens (human) 240 ALOX5 mutant phenotype evidence used in manual assertion
  • PMID:17394438
DOID:1612 breast cancer HGNC:651 Homo sapiens (human) 374 AREG mutant phenotype evidence used in manual assertion
  • PMID:16438846
DOID:5409 lung small cell carcinoma HGNC:3113 Homo sapiens (human) 1869 E2F1 mutant phenotype evidence used in manual assertion
  • PMID:23792570
DOID:3083 chronic obstructive pulmonary disease HGNC:2707 Homo sapiens (human) 1636 ACE mutant phenotype evidence used in manual assertion
  • PMID:19493329
  • PMID:20096799
DOID:3042 allergic contact dermatitis HGNC:1602 Homo sapiens (human) 1230 CCR1 mutant phenotype evidence used in manual assertion
  • PMID:18844696
DOID:6432 pulmonary hypertension RGD:2802 Rattus norvegicus (Norway rat) 25459 Hmgb1 mutant phenotype evidence used in manual assertion
  • PMID:25032709
DOID:2921 glomerulonephritis RGD:2493 Rattus norvegicus (Norway rat) 24310 Ace mutant phenotype evidence used in manual assertion
  • PMID:19164508
DOID:2799 bronchiolitis obliterans HGNC:3176 Homo sapiens (human) 1906 EDN1 mutant phenotype evidence used in manual assertion
  • PMID:9595474
DOID:10283 prostate cancer HGNC:1100 Homo sapiens (human) 672 BRCA1 mutant phenotype evidence used in manual assertion
  • PMID:17384678
DOID:3748 esophagus squamous cell carcinoma HGNC:1455 Homo sapiens (human) 811 CALR mutant phenotype evidence used in manual assertion
  • PMID:19684620
  • PMID:23814025
DOID:684 hepatocellular carcinoma HGNC:6866 Homo sapiens (human) 9448 MAP4K4 mutant phenotype evidence used in manual assertion
  • PMID:21196414
  • PMID:27010469
DOID:9538 multiple myeloma HGNC:4922 Homo sapiens (human) 3098 HK1 mutant phenotype evidence used in manual assertion
  • PMID:19996089
DOID:5520 head and neck squamous cell carcinoma HGNC:6205 Homo sapiens (human) 3726 JUNB mutant phenotype evidence used in manual assertion
  • PMID:26754630
DOID:4195 hyperglycemia RGD:3001 Rattus norvegicus (Norway rat) 24536 Lepr mutant phenotype evidence used in manual assertion
  • PMID:26537785
DOID:3347 osteosarcoma HGNC:3113 Homo sapiens (human) 1869 E2F1 mutant phenotype evidence used in manual assertion
  • PMID:29039472
DOID:365 bladder disease HGNC:1952 Homo sapiens (human) 1131 CHRM3 mutant phenotype evidence used in manual assertion
  • PMID:17922784
DOID:0080199 colorectal carcinoma HGNC:9801 Homo sapiens (human) 5879 RAC1 mutant phenotype evidence used in manual assertion
  • PMID:23559092
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Last updated: December 8, 2025