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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 10026 - 10050 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▲ Evidence References
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:12306 vitiligo HGNC:5438 Homo sapiens (human) 3458 IFNG inference by association of genotype from phenotype used in manual assertion
  • PMID:23777204
DOID:0050741 alcohol dependence HGNC:2303 Homo sapiens (human) 1363 CPE inference by association of genotype from phenotype used in manual assertion
  • PMID:20201924
  • PMID:27151647
DOID:14067 Plasmodium falciparum malaria HGNC:5141 Homo sapiens (human) 3240 HP inference by association of genotype from phenotype used in manual assertion
  • PMID:24478401
DOID:0060732 chromosome 9p deletion syndrome MGI:2670972 Mus musculus (house mouse) 329872 Frem1 author statement supported by traceable reference
  • PMID:21931569
DOID:0080238 autosomal dominant intellectual developmental disorder 47 HGNC:11354 Homo sapiens (human) 10274 STAG1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0081292 traumatic brain injury RGD:1598328 Rattus norvegicus (Norway rat) 310738 Ngf mutant phenotype evidence used in manual assertion
  • PMID:26285082
DOID:0070123 congenital nongoitrous hypothyroidism 4 HGNC:12372 Homo sapiens (human) 7252 TSHB inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050469 Costello syndrome HGNC:5173 Homo sapiens (human) 3265 HRAS inference by association of genotype from phenotype used in manual assertion
  • PMID:16170316
  • PMID:16881968
  • PMID:25914166
  • RGD:7240710
DOID:418 systemic scleroderma HGNC:3327 Homo sapiens (human) 2006 ELN direct assay evidence used in manual assertion
  • PMID:22563211
DOID:0060246 MASA syndrome WB:WBGene00002243 Caenorhabditis elegans 177078 lad-2 mutant phenotype evidence used in manual assertion
  • PMID:18195110
DOID:8866 actinic keratosis HGNC:8101 Homo sapiens (human) 4948 OCA2 inference by association of genotype from phenotype used in manual assertion
  • PMID:24617981
DOID:8893 psoriasis HGNC:43 Homo sapiens (human) 6890 TAP1 inference by association of genotype from phenotype used in manual assertion
  • PMID:11194890
DOID:0060578 Noonan syndrome 1 HGNC:9644 Homo sapiens (human) 5781 PTPN11 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:10763 hypertension HGNC:243 Homo sapiens (human) 118 ADD1 inference by association of genotype from phenotype used in manual assertion
  • PMID:9149697
DOID:784 chronic kidney disease RGD:3001 Rattus norvegicus (Norway rat) 24536 Lepr mutant phenotype evidence used in manual assertion
  • PMID:27465994
  • PMID:32390513
DOID:10286 prostate carcinoma HGNC:9393 Homo sapiens (human) 5578 PRKCA mutant phenotype evidence used in manual assertion
  • PMID:9474241
DOID:3082 interstitial lung disease HGNC:7176 Homo sapiens (human) 4318 MMP9 direct assay evidence used in manual assertion
  • PMID:20185904
DOID:980 choroidal sclerosis HGNC:4689 Homo sapiens (human) 3000 GUCY2D inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9351 diabetes mellitus HGNC:613 Homo sapiens (human) 348 APOE direct assay evidence used in manual assertion
  • PMID:17192461
DOID:0110739 neurodegeneration with brain iron accumulation 5 HGNC:28912 Homo sapiens (human) 11152 WDR45 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:10652 Alzheimer's disease HGNC:5233 Homo sapiens (human) 3304 HSPA1B inference by association of genotype from phenotype used in manual assertion
  • PMID:12967056
DOID:3410 carotid artery thrombosis HGNC:11784 Homo sapiens (human) 7056 THBD mutant phenotype evidence used in manual assertion
  • PMID:21885846
DOID:6432 pulmonary hypertension RGD:2536 Rattus norvegicus (Norway rat) 50672 Ednrb direct assay evidence used in manual assertion
  • PMID:15243299
DOID:0081267 graft-versus-host disease HGNC:6001 Homo sapiens (human) 3558 IL2 direct assay evidence used in manual assertion
  • PMID:8704686
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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