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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 126 - 150 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence References
DOID:12401 intermittent explosive disorder HGNC:2228 Homo sapiens (human) 1312 COMT inference by association of genotype from phenotype used in manual assertion
  • PMID:11204347
DOID:0050709 early infantile epileptic encephalopathy SGD:S000005662 Saccharomyces cerevisiae S288C 854303 IDH2 sequence similarity evidence used in manual assertion
  • PMID:28058510
DOID:520 aortic disease HGNC:6770 Homo sapiens (human) 4089 SMAD4 inference by association of genotype from phenotype used in manual assertion
  • PMID:25931195
DOID:0060304 dyschromatosis universalis hereditaria HGNC:47 Homo sapiens (human) 10058 ABCB6 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110971 brachydactyly type D HGNC:5136 Homo sapiens (human) 3239 HOXD13 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9256 colorectal cancer HGNC:8033 Homo sapiens (human) 4916 NTRK3 direct assay evidence used in manual assertion
  • PMID:28105243
  • PMID:33593392
DOID:1612 breast cancer HGNC:10850 Homo sapiens (human) 6470 SHMT1 inference by association of genotype from phenotype used in manual assertion
  • PMID:17896178
DOID:684 hepatocellular carcinoma HGNC:2707 Homo sapiens (human) 1636 ACE inference by association of genotype from phenotype used in manual assertion
  • PMID:25208933
DOID:5419 schizophrenia MGI:95627 Mus musculus (house mouse) 232333 Slc6a1 author statement supported by traceable reference
  • PMID:23922840
DOID:0060074 ductal carcinoma in situ HGNC:8591 Homo sapiens (human) 5062 PAK2 direct assay evidence used in manual assertion
  • PMID:22886747
DOID:4448 macular degeneration HGNC:5394 Homo sapiens (human) 3426 CFI inference by association of genotype from phenotype used in manual assertion
  • PMID:22815349
  • PMID:23685748
DOID:418 systemic scleroderma HGNC:6709 Homo sapiens (human) 4049 LTA inference by association of genotype from phenotype used in manual assertion
  • PMID:10600011
DOID:1470 major depressive disorder HGNC:6018 Homo sapiens (human) 3569 IL6 inference by association of genotype from phenotype used in manual assertion
  • PMID:30734130
DOID:9256 colorectal cancer HGNC:4944 Homo sapiens (human) 3119 HLA-DQB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:31001878
DOID:3490 Noonan syndrome HGNC:11187 Homo sapiens (human) 6654 SOS1 inference by association of genotype from phenotype used in manual assertion
  • PMID:20683980
DOID:11394 adult respiratory distress syndrome RGD:620537 Rattus norvegicus (Norway rat) 84007 C3ar1 mutant phenotype evidence used in manual assertion
  • PMID:16782534
DOID:0080177 hepatic veno-occlusive disease HGNC:4886 Homo sapiens (human) 3077 HFE inference by association of genotype from phenotype used in manual assertion
  • PMID:15834437
DOID:1793 pancreatic cancer HGNC:1100 Homo sapiens (human) 672 BRCA1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110248 cataract 30 HGNC:12692 Homo sapiens (human) 7431 VIM inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0060196 amyotrophic lateral sclerosis type 4 MGI:2443480 Mus musculus (house mouse) 269254 Setx author statement supported by traceable reference
  • PMID:29725819
DOID:9119 acute myeloid leukemia HGNC:7646 Homo sapiens (human) 10 NAT2 inference by association of genotype from phenotype used in manual assertion
  • PMID:21888617
DOID:8991 cervix uteri carcinoma in situ HGNC:1748 Homo sapiens (human) 999 CDH1 direct assay evidence used in manual assertion
  • PMID:17894941
DOID:9351 diabetes mellitus HGNC:2433 Homo sapiens (human) 1436 CSF1R direct assay evidence used in manual assertion
  • PMID:32724427
DOID:0080212 polycystic kidney disease 4 HGNC:9016 Homo sapiens (human) 5314 PKHD1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110383 retinitis pigmentosa 7 HGNC:9942 Homo sapiens (human) 5961 PRPH2 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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Last updated: December 8, 2025