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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 13976 - 14000 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▲ Evidence References
DOID:0050696 fetal alcohol spectrum disorder HGNC:9201 Homo sapiens (human) 5443 POMC direct assay evidence used in manual assertion
  • PMID:31329297
DOID:5517 stomach carcinoma HGNC:18505 Homo sapiens (human) 54894 RNF43 inference by association of genotype from phenotype used in manual assertion
  • PMID:24816253
DOID:0110338 osteogenesis imperfecta type 17 HGNC:11219 Homo sapiens (human) 6678 SPARC inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:12531 von Willebrand's disease MGI:98941 Mus musculus (house mouse) 22371 Vwf author statement supported by traceable reference
  • PMID:30565388
DOID:14503 neuronal ceroid lipofuscinosis FB:FBgn0086676 Drosophila melanogaster (fruit fly) 45380 spin combinatorial experimental and author inference evidence used in manual assertion
  • PMID:29046397
DOID:10763 hypertension RGD:61276 Rattus norvegicus (Norway rat) 58959 Crhr1 direct assay evidence used in manual assertion
  • PMID:11036160
DOID:3083 chronic obstructive pulmonary disease HGNC:8941 Homo sapiens (human) 5265 SERPINA1 inference by association of genotype from phenotype used in manual assertion
  • PMID:20298391
DOID:12185 otosclerosis HGNC:2197 Homo sapiens (human) 1277 COL1A1 inference by association of genotype from phenotype used in manual assertion
  • PMID:17489845
DOID:1123 spondyloarthropathy HGNC:4932 Homo sapiens (human) 3106 HLA-B inference by association of genotype from phenotype used in manual assertion
  • PMID:2257626
DOID:4552 large cell carcinoma HGNC:30796 Homo sapiens (human) 11171 STRAP direct assay evidence used in manual assertion
  • PMID:16778189
DOID:0111730 familial episodic pain syndrome 2 HGNC:10582 Homo sapiens (human) 6336 SCN10A inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050866 oral squamous cell carcinoma HGNC:6001 Homo sapiens (human) 3558 IL2 direct assay evidence used in manual assertion
  • PMID:10389944
DOID:10808 gastric ulcer RGD:620349 Rattus norvegicus (Norway rat) 29527 Ptgs2 mutant phenotype evidence used in manual assertion
  • PMID:17673547
DOID:4480 achondroplasia MGI:97372 Mus musculus (house mouse) 230103 Npr2 author statement supported by traceable reference
  • MGI:2152911
  • MGI:4947088
  • MGI:75337
DOID:9976 heroin dependence HGNC:277 Homo sapiens (human) 148 ADRA1A inference by association of genotype from phenotype used in manual assertion
  • PMID:33577997
DOID:2741 bilirubin metabolic disorder HGNC:12530 Homo sapiens (human) 54658 UGT1A1 direct assay evidence used in manual assertion
  • PMID:15753292
  • PMID:16609363
  • PMID:21993917
DOID:0060468 Holt-Oram syndrome HGNC:15924 Homo sapiens (human) 57167 SALL4 inference by association of genotype from phenotype used in manual assertion
  • PMID:12843316
DOID:3393 coronary artery disease HGNC:13916 Homo sapiens (human) 55937 APOM inference by association of genotype from phenotype used in manual assertion
  • PMID:17674965
DOID:0050864 non-arteritic anterior ischemic optic neuropathy HGNC:4439 Homo sapiens (human) 2811 GP1BA inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:2349 arteriosclerosis HGNC:6522 Homo sapiens (human) 3931 LCAT inference by association of genotype from phenotype used in manual assertion
  • PMID:12673583
DOID:3908 lung non-small cell carcinoma HGNC:1957 Homo sapiens (human) 1136 CHRNA3 inference by association of genotype from phenotype used in manual assertion
  • PMID:22722785
DOID:1884 viral hepatitis HGNC:6001 Homo sapiens (human) 3558 IL2 inference by association of genotype from phenotype used in manual assertion
  • PMID:21162873
DOID:0111969 immunodeficiency 39 HGNC:6122 Homo sapiens (human) 3665 IRF7 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:4440 seminoma HGNC:9221 Homo sapiens (human) 5460 POU5F1 direct assay evidence used in manual assertion
  • PMID:17549357
DOID:10534 stomach cancer HGNC:6024 Homo sapiens (human) 3575 IL7R inference by association of genotype from phenotype used in manual assertion
  • PMID:18687755
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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: December 8, 2025