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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 10076 - 10100 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▲ Evidence References
DOID:5419 schizophrenia HGNC:3024 Homo sapiens (human) 1814 DRD3 inference by association of genotype from phenotype used in manual assertion
  • PMID:1362221
  • RGD:7240710
DOID:12449 aplastic anemia HGNC:11892 Homo sapiens (human) 7124 TNF inference by association of genotype from phenotype used in manual assertion
  • PMID:12941546
DOID:3602 toxic encephalopathy HGNC:74 Homo sapiens (human) 9429 ABCG2 inference by association of genotype from phenotype used in manual assertion
  • PMID:17938643
DOID:1793 pancreatic cancer HGNC:12539 Homo sapiens (human) 54577 UGT1A7 inference by association of genotype from phenotype used in manual assertion
  • PMID:12806614
DOID:1727 retinal vein occlusion HGNC:9204 Homo sapiens (human) 5444 PON1 inference by association of genotype from phenotype used in manual assertion
  • PMID:23441121
DOID:4450 renal cell carcinoma HGNC:9955 Homo sapiens (human) 5970 RELA mutant phenotype evidence used in manual assertion
  • PMID:17290398
DOID:2316 brain ischemia RGD:620349 Rattus norvegicus (Norway rat) 29527 Ptgs2 direct assay evidence used in manual assertion
  • PMID:12535784
DOID:9675 pulmonary emphysema HGNC:7155 Homo sapiens (human) 4312 MMP1 inference by association of genotype from phenotype used in manual assertion
  • PMID:17363767
DOID:2377 multiple sclerosis HGNC:4944 Homo sapiens (human) 3119 HLA-DQB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:15201511
  • PMID:20463743
  • PMID:21741664
  • PMID:21908482
  • RGD:7240710
DOID:0060572 Ritscher-Schinzel syndrome 2 HGNC:28909 Homo sapiens (human) 28952 CCDC22 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050793 short QT syndrome HGNC:6251 Homo sapiens (human) 3757 KCNH2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:2394 ovarian cancer HGNC:11180 Homo sapiens (human) 6648 SOD2 direct assay evidence used in manual assertion
  • PMID:16179351
DOID:5844 myocardial infarction HGNC:5141 Homo sapiens (human) 3240 HP inference by association of genotype from phenotype used in manual assertion
  • PMID:2613263
  • PMID:3990081
DOID:0050800 cerebral creatine deficiency syndrome 1 MGI:2147834 Mus musculus (house mouse) 102857 Slc6a8 author statement supported by traceable reference
  • PMID:21249153
  • PMID:22751104
  • PMID:25485098
  • PMID:27466184
  • PMID:30013483
DOID:0110202 Charcot-Marie-Tooth disease dominant intermediate A HGNC:4181 Homo sapiens (human) 8729 GBF1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:684 hepatocellular carcinoma HGNC:30635 Homo sapiens (human) 11063 SOX30 direct assay evidence used in manual assertion
  • PMID:30312695
DOID:0111633 congenital sucrase-isomaltase deficiency HGNC:10856 Homo sapiens (human) 6476 SI inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050560 Walker-Warburg syndrome HGNC:19139 Homo sapiens (human) 55624 POMGNT1 inference by association of genotype from phenotype used in manual assertion
  • PMID:11709191
  • PMID:15236414
  • PMID:22554691
  • PMID:23689641
DOID:12140 Chagas disease HGNC:5237 Homo sapiens (human) 3308 HSPA4 direct assay evidence used in manual assertion
  • PMID:21801456
DOID:3908 lung non-small cell carcinoma HGNC:1383 Homo sapiens (human) 768 CA9 genetic interaction evidence used in manual assertion
  • PMID:23910904
DOID:12858 Huntington's disease HGNC:4586 Homo sapiens (human) 2904 GRIN2B inference by association of genotype from phenotype used in manual assertion
  • PMID:15742215
  • PMID:17569088
DOID:9975 cocaine dependence HGNC:1957 Homo sapiens (human) 1136 CHRNA3 inference by association of genotype from phenotype used in manual assertion
  • PMID:24057674
DOID:1790 malignant mesothelioma HGNC:12828 Homo sapiens (human) 7515 XRCC1 inference by association of genotype from phenotype used in manual assertion
  • PMID:22982660
DOID:5844 myocardial infarction HGNC:286 Homo sapiens (human) 154 ADRB2 inference by association of genotype from phenotype used in manual assertion
  • PMID:15520258
DOID:526 human immunodeficiency virus infectious disease HGNC:1603 Homo sapiens (human) 729230 CCR2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
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Supported by JST NBDC Grant Number JPMJND2204

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