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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 101 - 125 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▲ FlyGlycoDB Evidence References
DOID:9352 type 2 diabetes mellitus HGNC:59 Homo sapiens (human) 6833 ABCC8 inference by association of genotype from phenotype used in manual assertion
  • PMID:11030411
  • PMID:15579791
  • PMID:17259403
  • PMID:18346985
  • PMID:18599530
  • PMID:18664331
  • RGD:7240710
DOID:2018 hyperinsulinism HGNC:59 Homo sapiens (human) 6833 ABCC8 inference by association of genotype from phenotype used in manual assertion
  • PMID:12199344
DOID:12930 dilated cardiomyopathy HGNC:60 Homo sapiens (human) 10060 ABCC9 inference by association of genotype from phenotype used in manual assertion
  • PMID:15034580
DOID:0070600 intellectual disability and myopathy syndrome HGNC:60 Homo sapiens (human) 10060 ABCC9 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110451 dilated cardiomyopathy 1O HGNC:60 Homo sapiens (human) 10060 ABCC9 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050650 familial atrial fibrillation HGNC:60 Homo sapiens (human) 10060 ABCC9 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0060569 hypertrichotic osteochondrodysplasia Cantu type HGNC:60 Homo sapiens (human) 10060 ABCC9 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:10588 adrenoleukodystrophy HGNC:61 Homo sapiens (human) 215 ABCD1 inference by association of genotype from phenotype used in manual assertion
  • PMID:8048932
  • RGD:7240710
DOID:0111066 congenital bile acid synthesis defect 5 HGNC:67 Homo sapiens (human) 5825 ABCD3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:905 Zellweger syndrome HGNC:67 Homo sapiens (human) 5825 ABCD3 inference by association of genotype from phenotype used in manual assertion
  • PMID:1301993
DOID:526 human immunodeficiency virus infectious disease HGNC:69 Homo sapiens (human) 6059 ABCE1 inference by association of genotype from phenotype used in manual assertion
  • PMID:19657357
DOID:13189 gout HGNC:74 Homo sapiens (human) 9429 ABCG2 inference by association of genotype from phenotype used in manual assertion
  • PMID:19506252
  • RGD:7240710
DOID:8552 chronic myeloid leukemia HGNC:74 Homo sapiens (human) 9429 ABCG2 inference by association of genotype from phenotype used in manual assertion
  • PMID:24123600
  • PMID:24581936
  • PMID:26250462
DOID:9538 multiple myeloma HGNC:74 Homo sapiens (human) 9429 ABCG2 mutant phenotype evidence used in manual assertion
  • PMID:26314844
DOID:4450 renal cell carcinoma HGNC:74 Homo sapiens (human) 9429 ABCG2 inference by association of genotype from phenotype used in manual assertion
  • PMID:15906349
DOID:707 B-cell lymphoma HGNC:74 Homo sapiens (human) 9429 ABCG2 inference by association of genotype from phenotype used in manual assertion
  • PMID:21918980
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:0060983 sitosterolemia 2 HGNC:13886 Homo sapiens (human) 64240 ABCG5 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:2349 arteriosclerosis HGNC:13886 Homo sapiens (human) 64240 ABCG5 inference by association of genotype from phenotype used in manual assertion
  • PMID:11099417
DOID:0090019 sitosterolemia 1 HGNC:13886 Homo sapiens (human) 64240 ABCG5 inference by association of genotype from phenotype used in manual assertion
  • PMID:11452359
DOID:9970 obesity HGNC:13887 Homo sapiens (human) 64241 ABCG8 inference by association of genotype from phenotype used in manual assertion
  • PMID:15331430
DOID:1168 familial hyperlipidemia HGNC:13887 Homo sapiens (human) 64241 ABCG8 inference by association of genotype from phenotype used in manual assertion
  • PMID:12671028
DOID:2349 arteriosclerosis HGNC:13887 Homo sapiens (human) 64241 ABCG8 inference by association of genotype from phenotype used in manual assertion
  • PMID:11099417
DOID:0090019 sitosterolemia 1 HGNC:13887 Homo sapiens (human) 64241 ABCG8 inference by association of genotype from phenotype used in manual assertion
  • PMID:11099417
  • PMID:11452359
  • RGD:7240710
DOID:0080181 PHARC syndrome HGNC:15868 Homo sapiens (human) 26090 ABHD12 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
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