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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 13501 - 13525 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▲ Evidence References
DOID:12930 dilated cardiomyopathy HGNC:4886 Homo sapiens (human) 3077 HFE inference by association of genotype from phenotype used in manual assertion
  • PMID:11040018
DOID:0050591 tooth agenesis HGNC:1069 Homo sapiens (human) 650 BMP2 inference by association of genotype from phenotype used in manual assertion
  • PMID:23079991
DOID:0060307 autosomal dominant intellectual developmental disorder HGNC:22474 Homo sapiens (human) 9969 MED13 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0060193 amyotrophic lateral sclerosis type 1 HGNC:9461 Homo sapiens (human) 5630 PRPH inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050437 Danon disease MGI:96748 Mus musculus (house mouse) 16784 Lamp2 author statement supported by traceable reference
  • PMID:10972293
  • PMID:28526246
  • PMID:34459252
DOID:9970 obesity HGNC:4267 Homo sapiens (human) 2693 GHSR inference by association of genotype from phenotype used in manual assertion
  • PMID:16511600
DOID:0111068 congenital bile acid synthesis defect 4 HGNC:451 Homo sapiens (human) 23600 AMACR inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:8924 autoimmune thrombocytopenic purpura HGNC:6014 Homo sapiens (human) 3565 IL4 inference by association of genotype from phenotype used in manual assertion
  • PMID:25051072
DOID:10983 Alport syndrome HGNC:2207 Homo sapiens (human) 1287 COL4A5 inference by association of genotype from phenotype used in manual assertion
  • PMID:2349482
DOID:3021 acute kidney failure HGNC:320 Homo sapiens (human) 177 AGER direct assay evidence used in manual assertion
  • PMID:21811803
DOID:1909 melanoma HGNC:11920 Homo sapiens (human) 355 FAS inference by association of genotype from phenotype used in manual assertion
  • PMID:16538172
DOID:0111743 cerebellar ataxia type 47 HGNC:14957 Homo sapiens (human) 9698 PUM1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:2048 autoimmune hepatitis HGNC:4944 Homo sapiens (human) 3119 HLA-DQB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:17050030
  • PMID:20007077
DOID:0050589 inflammatory bowel disease HGNC:5344 Homo sapiens (human) 3383 ICAM1 inference by association of genotype from phenotype used in manual assertion
  • PMID:15638228
DOID:10825 essential hypertension HGNC:336 Homo sapiens (human) 185 AGTR1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110865 congenital stationary night blindness 1B MGI:1351343 Mus musculus (house mouse) 108072 Grm6 author statement supported by traceable reference
  • PMID:26241901
  • PMID:28490646
DOID:0111385 inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1 HGNC:12666 Homo sapiens (human) 7415 VCP inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0060582 Noonan syndrome 4 HGNC:11187 Homo sapiens (human) 6654 SOS1 inference by association of genotype from phenotype used in manual assertion
  • PMID:17143282
  • PMID:17143285
  • PMID:17586837
  • RGD:7240710
DOID:4724 brain edema RGD:619991 Rattus norvegicus (Norway rat) 83785 Vegfa direct assay evidence used in manual assertion
  • PMID:15879344
DOID:14320 generalized anxiety disorder FB:FBgn0263116 Drosophila melanogaster (fruit fly) 37191 5-HT1B combinatorial experimental and author inference evidence used in manual assertion
  • PMID:27020741
DOID:0080205 CAKUT HGNC:8001 Homo sapiens (human) 8204 NRIP1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080600 COVID-19 HGNC:7 Homo sapiens (human) 2 A2M inference by association of genotype from phenotype used in manual assertion
  • PMID:32747830
DOID:627 severe combined immunodeficiency HGNC:11566 Homo sapiens (human) 6892 TAPBP inference by association of genotype from phenotype used in manual assertion
  • PMID:12149238
DOID:684 hepatocellular carcinoma HGNC:7989 Homo sapiens (human) 4893 NRAS genetic interaction evidence used in manual assertion
  • PMID:21993994
DOID:7148 rheumatoid arthritis HGNC:6001 Homo sapiens (human) 3558 IL2 direct assay evidence used in manual assertion
  • PMID:6421522
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Supported by JST NBDC Grant Number JPMJND2204

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Last updated: December 8, 2025