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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 10401 - 10425 of 14279 in total
Disease ID ▲ Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence References
DOID:3525 middle cerebral artery infarction RGD:2143 Rattus norvegicus (Norway rat) 25293 Aqp4 mutant phenotype evidence used in manual assertion
  • PMID:33127515
DOID:3525 middle cerebral artery infarction RGD:620360 Rattus norvegicus (Norway rat) 83619 Nfe2l2 direct assay evidence used in manual assertion
  • PMID:23880501
  • PMID:24466583
DOID:3525 middle cerebral artery infarction RGD:70982 Rattus norvegicus (Norway rat) 84027 Gsk3b direct assay evidence used in manual assertion
  • PMID:28440874
DOID:3525 middle cerebral artery infarction RGD:3177 Rattus norvegicus (Norway rat) 24596 Ngfr direct assay evidence used in manual assertion
  • PMID:22678884
DOID:3525 middle cerebral artery infarction RGD:621397 Rattus norvegicus (Norway rat) 84022 Ghsr mutant phenotype evidence used in manual assertion
  • PMID:19352052
DOID:3525 middle cerebral artery infarction HGNC:6000 Homo sapiens (human) 3557 IL1RN mutant phenotype evidence used in manual assertion
  • PMID:7790404
DOID:3525 middle cerebral artery infarction HGNC:3415 Homo sapiens (human) 2056 EPO direct assay evidence used in manual assertion
  • PMID:20833153
DOID:3525 middle cerebral artery infarction HGNC:3530 Homo sapiens (human) 2161 F12 direct assay evidence used in manual assertion
  • PMID:16533887
DOID:3525 middle cerebral artery infarction RGD:1598328 Rattus norvegicus (Norway rat) 310738 Ngf mutant phenotype evidence used in manual assertion
  • PMID:29409115
DOID:3525 middle cerebral artery infarction RGD:620103 Rattus norvegicus (Norway rat) 64639 Bad direct assay evidence used in manual assertion
  • PMID:21891976
  • PMID:22200499
DOID:3525 middle cerebral artery infarction RGD:3876 Rattus norvegicus (Norway rat) 24835 Tnf mutant phenotype evidence used in manual assertion
  • PMID:15647744
DOID:3525 middle cerebral artery infarction RGD:2661 Rattus norvegicus (Norway rat) 24383 Gapdh direct assay evidence used in manual assertion
  • PMID:25882840
DOID:3525 middle cerebral artery infarction HGNC:2438 Homo sapiens (human) 1440 CSF3 direct assay evidence used in manual assertion
  • PMID:19298757
DOID:3525 middle cerebral artery infarction HGNC:10848 Homo sapiens (human) 6469 SHH direct assay evidence used in manual assertion
  • PMID:22324418
DOID:3525 middle cerebral artery infarction HGNC:16369 Homo sapiens (human) 11315 PARK7 direct assay evidence used in manual assertion
  • PMID:17882163
DOID:3525 middle cerebral artery infarction HGNC:3415 Homo sapiens (human) 2056 EPO mutant phenotype evidence used in manual assertion
  • PMID:20547143
DOID:3525 middle cerebral artery infarction RGD:2677 Rattus norvegicus (Norway rat) 25453 Gdnf mutant phenotype evidence used in manual assertion
  • PMID:29497380
DOID:3525 middle cerebral artery infarction RGD:621237 Rattus norvegicus (Norway rat) 25625 Tnfrsf1a mutant phenotype evidence used in manual assertion
  • PMID:15647744
DOID:3525 middle cerebral artery infarction RGD:3786 Rattus norvegicus (Norway rat) 25559 Abcc8 mutant phenotype evidence used in manual assertion
  • PMID:23149556
  • PMID:24602692
DOID:3525 middle cerebral artery infarction RGD:620218 Rattus norvegicus (Norway rat) 81646 Creb1 direct assay evidence used in manual assertion
  • PMID:35218623
DOID:3525 middle cerebral artery infarction RGD:3035 Rattus norvegicus (Norway rat) 29409 Mag mutant phenotype evidence used in manual assertion
  • PMID:15678116
DOID:3525 middle cerebral artery infarction RGD:631365 Rattus norvegicus (Norway rat) 297508 Nampt mutant phenotype evidence used in manual assertion
  • PMID:28495827
DOID:3525 middle cerebral artery infarction RGD:619991 Rattus norvegicus (Norway rat) 83785 Vegfa mutant phenotype evidence used in manual assertion
  • PMID:29497380
DOID:3525 middle cerebral artery infarction RGD:2283 Rattus norvegicus (Norway rat) 50662 Runx1 inference by association of genotype from phenotype used in manual assertion
  • PMID:24672479
DOID:3525 middle cerebral artery infarction RGD:2053 Rattus norvegicus (Norway rat) 25591 Parp1 direct assay evidence used in manual assertion
  • PMID:25882840

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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Supported by JST NBDC Grant Number JPMJND2204

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


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