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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 5776 - 5800 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence References
DOID:8947 diabetic retinopathy HGNC:613 Homo sapiens (human) 348 APOE inference by association of genotype from phenotype used in manual assertion
  • PMID:16862278
DOID:332 amyotrophic lateral sclerosis HGNC:613 Homo sapiens (human) 348 APOE inference by association of genotype from phenotype used in manual assertion
  • PMID:8899655
DOID:0080158 herpes simplex virus keratitis HGNC:613 Homo sapiens (human) 348 APOE direct assay evidence used in manual assertion
  • PMID:18515564
DOID:13809 familial combined hyperlipidemia HGNC:613 Homo sapiens (human) 348 APOE inference by association of genotype from phenotype used in manual assertion
  • PMID:12915220
  • PMID:17127808
DOID:0110042 Alzheimer's disease 3 HGNC:613 Homo sapiens (human) 348 APOE inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3526 cerebral infarction HGNC:613 Homo sapiens (human) 348 APOE inference by association of genotype from phenotype used in manual assertion
  • PMID:17016617
DOID:1936 atherosclerosis HGNC:613 Homo sapiens (human) 348 APOE mutant phenotype evidence used in manual assertion
  • PMID:7593602
DOID:13641 exfoliation syndrome HGNC:613 Homo sapiens (human) 348 APOE inference by association of genotype from phenotype used in manual assertion
  • PMID:15939044
DOID:3905 lung carcinoma HGNC:613 Homo sapiens (human) 348 APOE inference by association of genotype from phenotype used in manual assertion
  • PMID:24175756
DOID:4423 sea-blue histiocytosis HGNC:613 Homo sapiens (human) 348 APOE inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:5679 retinal disease HGNC:613 Homo sapiens (human) 348 APOE inference by association of genotype from phenotype used in manual assertion
  • PMID:17562993
DOID:9351 diabetes mellitus HGNC:613 Homo sapiens (human) 348 APOE direct assay evidence used in manual assertion
  • PMID:17192461
DOID:3145 hyperlipoproteinemia type III HGNC:613 Homo sapiens (human) 348 APOE inference by association of genotype from phenotype used in manual assertion
  • PMID:199847
  • PMID:7175379
  • RGD:7240710
DOID:1070 primary open angle glaucoma HGNC:613 Homo sapiens (human) 348 APOE inference by association of genotype from phenotype used in manual assertion
  • PMID:17706090
DOID:4448 macular degeneration HGNC:613 Homo sapiens (human) 348 APOE inference by association of genotype from phenotype used in manual assertion
  • PMID:12567264
  • PMID:19384966
DOID:4606 bile duct cancer HGNC:613 Homo sapiens (human) 348 APOE inference by association of genotype from phenotype used in manual assertion
  • PMID:18296645
DOID:10211 cholelithiasis HGNC:613 Homo sapiens (human) 348 APOE inference by association of genotype from phenotype used in manual assertion
  • PMID:18296645
DOID:12930 dilated cardiomyopathy HGNC:613 Homo sapiens (human) 348 APOE inference by association of genotype from phenotype used in manual assertion
  • PMID:16714771
DOID:1920 hyperuricemia HGNC:613 Homo sapiens (human) 348 APOE inference by association of genotype from phenotype used in manual assertion
  • PMID:15713714
DOID:13544 low tension glaucoma HGNC:613 Homo sapiens (human) 348 APOE inference by association of genotype from phenotype used in manual assertion
  • PMID:16778644
DOID:7693 abdominal aortic aneurysm HGNC:613 Homo sapiens (human) 348 APOE inference by association of genotype from phenotype used in manual assertion
  • PMID:10848855
DOID:10873 Kuhnt-Junius degeneration HGNC:613 Homo sapiens (human) 348 APOE inference by association of genotype from phenotype used in manual assertion
  • PMID:9512153
DOID:9538 multiple myeloma HGNC:613 Homo sapiens (human) 348 APOE direct assay evidence used in manual assertion
  • PMID:22348216
DOID:0111835 congenital nongoitrous hypothyroidism 9 HGNC:6128 Homo sapiens (human) 8471 IRS4 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:1324 lung cancer HGNC:6128 Homo sapiens (human) 8471 IRS4 mutant phenotype evidence used in manual assertion
  • PMID:33894221
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: April 7, 2025