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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 9826 - 9850 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▲ FlyGlycoDB Evidence References
DOID:0060316 orofaciodigital syndrome I MGI:1350328 Mus musculus (house mouse) 237222 Ofd1 author statement supported by traceable reference
  • PMID:16311594
DOID:5212 congenital disorder of glycosylation MGI:1339639 Mus musculus (house mouse) 108155 Ogt author statement supported by traceable reference
  • PMID:38566589
DOID:0050679 blue cone monochromacy MGI:1097692 Mus musculus (house mouse) 14539 Opn1mw author statement supported by traceable reference
  • PMID:28751656
DOID:1574 alcohol use disorder RGD:3233 Rattus norvegicus (Norway rat) 24613 Oprd1 mutant phenotype evidence used in manual assertion
  • PMID:7501658
DOID:5844 myocardial infarction RGD:3233 Rattus norvegicus (Norway rat) 24613 Oprd1 direct assay evidence used in manual assertion
  • PMID:12798419
DOID:5844 myocardial infarction RGD:3233 Rattus norvegicus (Norway rat) 24613 Oprd1 mutant phenotype evidence used in manual assertion
  • PMID:15076225
DOID:0060001 withdrawal disorder RGD:69426 Rattus norvegicus (Norway rat) 29335 Oprk1 mutant phenotype evidence used in manual assertion
  • PMID:22515275
DOID:9976 heroin dependence RGD:69426 Rattus norvegicus (Norway rat) 29335 Oprk1 mutant phenotype evidence used in manual assertion
  • PMID:24305833
  • PMID:24725195
DOID:5844 myocardial infarction RGD:69426 Rattus norvegicus (Norway rat) 29335 Oprk1 mutant phenotype evidence used in manual assertion
  • PMID:15076225
DOID:1574 alcohol use disorder RGD:68438 Rattus norvegicus (Norway rat) 29256 Oprl1 mutant phenotype evidence used in manual assertion
  • PMID:11814626
DOID:9970 obesity RGD:3234 Rattus norvegicus (Norway rat) 25601 Oprm1 mutant phenotype evidence used in manual assertion
  • PMID:16876155
DOID:0060041 autism spectrum disorder MGI:97441 Mus musculus (house mouse) 18390 Oprm1 author statement supported by traceable reference
  • PMID:20503133
DOID:10273 heart conduction disease FB:FBgn0017561 Drosophila melanogaster (fruit fly) 32020 Ork1 combinatorial experimental and author inference evidence used in manual assertion
  • PMID:16890525
DOID:10283 prostate cancer FB:FBgn0032015 Drosophila melanogaster (fruit fly) 34137 Ostgamma CG7830 combinatorial experimental and author inference evidence used in manual assertion
  • PMID:25117438
DOID:0110939 autosomal recessive osteopetrosis 5 MGI:2655574 Mus musculus (house mouse) 14628 Ostm1 author statement supported by traceable reference
  • PMID:1155801
DOID:10283 prostate cancer FB:FBgn0032015 Drosophila melanogaster (fruit fly) 34137 Ostγ CG7830 combinatorial experimental and author inference evidence used in manual assertion
  • PMID:25117438
DOID:0110480 autosomal recessive nonsyndromic deafness 22 MGI:2149209 Mus musculus (house mouse) 246190 Otoa author statement supported by traceable reference
  • PMID:23129639
DOID:0110474 autosomal recessive nonsyndromic deafness 18B MGI:1202064 Mus musculus (house mouse) 18419 Otog author statement supported by traceable reference
  • PMID:26636018
DOID:10808 gastric ulcer RGD:3239 Rattus norvegicus (Norway rat) 25342 Oxtr mutant phenotype evidence used in manual assertion
  • PMID:11764003
DOID:0110567 autosomal dominant nonsyndromic deafness 41 HGNC:15459 Homo sapiens (human) 22953 P2RX2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:6713 cerebrovascular disease HGNC:18124 Homo sapiens (human) 64805 P2RY12 inference by association of genotype from phenotype used in manual assertion
  • PMID:15933261
DOID:9352 type 2 diabetes mellitus HGNC:18124 Homo sapiens (human) 64805 P2RY12 mutant phenotype evidence used in manual assertion
  • PMID:15483100
DOID:0060692 platelet-type bleeding disorder 8 HGNC:18124 Homo sapiens (human) 64805 P2RY12 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050830 peripheral artery disease HGNC:18124 Homo sapiens (human) 64805 P2RY12 inference by association of genotype from phenotype used in manual assertion
  • PMID:14662702
DOID:2841 asthma HGNC:18124 Homo sapiens (human) 64805 P2RY12 inference by association of genotype from phenotype used in manual assertion
  • PMID:22010907

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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