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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 10051 - 10075 of 14279 in total
Disease ID Disease Name ▲ Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence References
DOID:5844 myocardial infarction HGNC:6701 Homo sapiens (human) 4043 LRPAP1 inference by association of genotype from phenotype used in manual assertion
  • PMID:12394648
DOID:5844 myocardial infarction RGD:69426 Rattus norvegicus (Norway rat) 29335 Oprk1 mutant phenotype evidence used in manual assertion
  • PMID:15076225
DOID:5844 myocardial infarction RGD:3645 Rattus norvegicus (Norway rat) 24770 Ccl2 direct assay evidence used in manual assertion
  • PMID:18753699
DOID:5844 myocardial infarction HGNC:543 Homo sapiens (human) 308 ANXA5 inference by association of genotype from phenotype used in manual assertion
  • PMID:12200370
DOID:5844 myocardial infarction HGNC:5141 Homo sapiens (human) 3240 HP inference by association of genotype from phenotype used in manual assertion
  • PMID:2613263
  • PMID:3990081
DOID:5844 myocardial infarction HGNC:286 Homo sapiens (human) 154 ADRB2 inference by association of genotype from phenotype used in manual assertion
  • PMID:15520258
DOID:5844 myocardial infarction HGNC:320 Homo sapiens (human) 177 AGER inference by association of genotype from phenotype used in manual assertion
  • PMID:16728681
DOID:5844 myocardial infarction HGNC:6709 Homo sapiens (human) 4049 LTA inference by association of genotype from phenotype used in manual assertion
  • PMID:12426569
  • PMID:23398946
  • RGD:7240710
DOID:5844 myocardial infarction RGD:2069 Rattus norvegicus (Norway rat) 24179 Agt direct assay evidence used in manual assertion
  • PMID:21167013
DOID:5844 myocardial infarction HGNC:6692 Homo sapiens (human) 4035 LRP1 inference by association of genotype from phenotype used in manual assertion
  • PMID:12402342
DOID:5844 myocardial infarction RGD:2536 Rattus norvegicus (Norway rat) 50672 Ednrb direct assay evidence used in manual assertion
  • PMID:12524016
DOID:5844 myocardial infarction HGNC:5962 Homo sapiens (human) 3586 IL10 inference by association of genotype from phenotype used in manual assertion
  • PMID:15466015
DOID:5844 myocardial infarction HGNC:333 Homo sapiens (human) 183 AGT inference by association of genotype from phenotype used in manual assertion
  • PMID:11393670
  • PMID:17299437
DOID:5844 myocardial infarction HGNC:8583 Homo sapiens (human) 5054 SERPINE1 inference by association of genotype from phenotype used in manual assertion
  • PMID:12477941
DOID:5844 myocardial infarction HGNC:24678 Homo sapiens (human) 79068 FTO inference by association of genotype from phenotype used in manual assertion
  • PMID:20031593
  • PMID:26772723
DOID:5844 myocardial infarction HGNC:3415 Homo sapiens (human) 2056 EPO direct assay evidence used in manual assertion
  • PMID:21415704
DOID:5844 myocardial infarction RGD:621576 Rattus norvegicus (Norway rat) 83531 Vdac2 direct assay evidence used in manual assertion
  • PMID:20601275
DOID:5844 myocardial infarction RGD:3249 Rattus norvegicus (Norway rat) 24617 Serpine1 mutant phenotype evidence used in manual assertion
  • PMID:16053971
DOID:5844 myocardial infarction HGNC:6562 Homo sapiens (human) 3957 LGALS2 inference by association of genotype from phenotype used in manual assertion
  • PMID:15129282
  • RGD:7240710
DOID:5844 myocardial infarction RGD:70982 Rattus norvegicus (Norway rat) 84027 Gsk3b mutant phenotype evidence used in manual assertion
  • PMID:16565311
DOID:5844 myocardial infarction HGNC:11850 Homo sapiens (human) 7099 TLR4 inference by association of genotype from phenotype used in manual assertion
  • PMID:15864121
  • PMID:18549840
DOID:5844 myocardial infarction HGNC:602 Homo sapiens (human) 337 APOA4 inference by association of genotype from phenotype used in manual assertion
  • PMID:7958503
DOID:5844 myocardial infarction RGD:3673 Rattus norvegicus (Norway rat) 29499 Shh mutant phenotype evidence used in manual assertion
  • PMID:20052412
DOID:5844 myocardial infarction HGNC:2202 Homo sapiens (human) 1282 COL4A1 inference by association of genotype from phenotype used in manual assertion
  • PMID:18077766
DOID:5844 myocardial infarction HGNC:11760 Homo sapiens (human) 7035 TFPI direct assay evidence used in manual assertion
  • PMID:15630488
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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