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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 October 9, 2024
Displaying entries 70801 - 70825 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▲ Evidence Code Names References
DOID:3393 coronary artery disease RGD:1310740 Rattus norvegicus (Norway rat) 291437 Lipg
  • MGI:6194238
DOID:9111 cutaneous leishmaniasis MGI:96537 Mus musculus (house mouse) 16153 Il10
  • MGI:6194238
DOID:0081267 graft-versus-host disease MGI:98279 Mus musculus (house mouse) 20343 Sell
  • MGI:6194238
DOID:0060284 paroxysmal nocturnal hemoglobinuria Xenbase:XB-GENE-996765 Xenopus tropicalis (tropical clawed frog) 100158632 piga
  • MGI:6194238
DOID:850 lung disease RGD:3667 Rattus norvegicus (Norway rat) 25350 Sftpd
  • MGI:6194238
  • PMID:17616020
DOID:0080301 atypical hemolytic-uremic syndrome HGNC:11784 Homo sapiens (human) 7056 THBD
  • PMID:19625716
  • PMID:20595690
  • RGD:7240710
DOID:1612 breast cancer FB:FBgn0004360 Drosophila melanogaster (fruit fly) 35975 Wnt2
  • MGI:6194238
DOID:684 hepatocellular carcinoma HGNC:1919 Homo sapiens (human) 1108 CHD4
  • PMID:26095183
DOID:10652 Alzheimer's disease HGNC:389 Homo sapiens (human) 8574 AKR7A2
  • PMID:11597610
DOID:264 hemangiopericytoma HGNC:6307 Homo sapiens (human) 3791 KDR
  • PMID:26951238
DOID:11044 gastroschisis MGI:96677 Mus musculus (house mouse) 16590 Kit
  • MGI:6194238
DOID:0090132 complex cortical dysplasia with other brain malformations 7 HGNC:12412 Homo sapiens (human) 7280 TUBB2A
  • MGI:6194238
DOID:3883 Lynch syndrome HGNC:10050 Homo sapiens (human) 6041 RNASEL
  • PMID:16054567
DOID:14735 hereditary angioedema HGNC:3544 Homo sapiens (human) 2155 F7
  • PMID:9129025
DOID:10283 prostate cancer HGNC:4566 Homo sapiens (human) 2885 GRB2
  • PMID:17372910
  • PMID:28930697
DOID:3021 acute kidney failure RGD:2185 Rattus norvegicus (Norway rat) 25107 Avpr1a
  • PMID:17347933
DOID:0111970 immunodeficiency 10 HGNC:11386 Homo sapiens (human) 6786 STIM1
  • RGD:7240710
DOID:1289 neurodegenerative disease HGNC:3084 Homo sapiens (human) 1855 DVL1
  • MGI:6194238
DOID:13413 hepatic encephalopathy HGNC:6091 Homo sapiens (human) 3643 INSR
  • MGI:6194238
DOID:6364 migraine MGI:99841 Mus musculus (house mouse) 15566 Htr7
  • MGI:6194238
DOID:5082 liver cirrhosis HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:20570631
  • PMID:26857650
DOID:1470 major depressive disorder RGD:69270 Rattus norvegicus (Norway rat) 85426 Slc5a7
  • MGI:6194238
DOID:3328 temporal lobe epilepsy WB:WBGene00012364 Caenorhabditis elegans 179991 zmp-4
  • MGI:6194238
DOID:3525 middle cerebral artery infarction ZFIN:ZDB-GENE-030115-1 Danio rerio (zebrafish) 317743 gapdh
  • MGI:6194238
DOID:3021 acute kidney failure WB:WBGene00007516 Caenorhabditis elegans 181178 gpx-5
  • MGI:6194238

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International Collaboration

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 9, 2024