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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 July 29, 2024
Displaying entries 2401 - 2425 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:14227 azoospermia WB:WBGene00002028 Caenorhabditis elegans 177675 hst-1
  • MGI:6194238
DOID:5154 borna disease WB:WBGene00004051 Caenorhabditis elegans 177683 parg-1
  • MGI:6194238
DOID:3454 brain infarction WB:WBGene00004051 Caenorhabditis elegans 177683 parg-1
  • MGI:6194238
DOID:0070352 stress-induced childhood-onset neurodegeneration with variable ataxia and seizures WB:WBGene00004051 Caenorhabditis elegans 177683 parg-1
  • MGI:6194238
DOID:0070254 congenital disorder of glycosylation type IIb WB:WBGene00008775 Caenorhabditis elegans 177998 mogs-1
  • MGI:6194238
DOID:2748 glycogen storage disease III HGNC:321 Homo sapiens (human) 178 AGL
  • MGI:6194238
  • PMID:16705713
  • RGD:7240710
DOID:4676 uremia HGNC:321 Homo sapiens (human) 178 AGL
  • MGI:6194238
DOID:1591 renovascular hypertension WB:WBGene00007108 Caenorhabditis elegans 178046 gspd-1
  • MGI:6194238
DOID:13628 favism WB:WBGene00007108 Caenorhabditis elegans 178046 gspd-1
  • MGI:6194238
DOID:2861 congenital nonspherocytic hemolytic anemia WB:WBGene00007108 Caenorhabditis elegans 178046 gspd-1
  • MGI:6194238
DOID:9279 hyperhomocysteinemia WB:WBGene00007108 Caenorhabditis elegans 178046 gspd-1
  • MGI:6194238
DOID:9351 diabetes mellitus WB:WBGene00007108 Caenorhabditis elegans 178046 gspd-1
  • MGI:6194238
DOID:0050328 congenital hypothyroidism WB:WBGene00007108 Caenorhabditis elegans 178046 gspd-1
  • MGI:6194238
DOID:684 hepatocellular carcinoma WB:WBGene00007108 Caenorhabditis elegans 178046 gspd-1
  • MGI:6194238
DOID:14067 Plasmodium falciparum malaria WB:WBGene00007108 Caenorhabditis elegans 178046 gspd-1
  • MGI:6194238
DOID:13580 cholestasis WB:WBGene00007108 Caenorhabditis elegans 178046 gspd-1
  • MGI:6194238
DOID:12365 malaria WB:WBGene00007108 Caenorhabditis elegans 178046 gspd-1
  • MGI:6194238
DOID:83 cataract WB:WBGene00007108 Caenorhabditis elegans 178046 gspd-1
  • MGI:6194238
DOID:224 transient cerebral ischemia WB:WBGene00007108 Caenorhabditis elegans 178046 gspd-1
  • MGI:6194238
DOID:2383 neonatal jaundice WB:WBGene00007108 Caenorhabditis elegans 178046 gspd-1
  • MGI:6194238
DOID:5844 myocardial infarction WB:WBGene00007108 Caenorhabditis elegans 178046 gspd-1
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus WB:WBGene00007108 Caenorhabditis elegans 178046 gspd-1
  • MGI:6194238
DOID:0080208 metabolic dysfunction-associated steatotic liver disease WB:WBGene00007108 Caenorhabditis elegans 178046 gspd-1
  • MGI:6194238
DOID:557 kidney disease WB:WBGene00007108 Caenorhabditis elegans 178046 gspd-1
  • MGI:6194238
DOID:9281 phenylketonuria WB:WBGene00007108 Caenorhabditis elegans 178046 gspd-1
  • MGI:6194238

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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: August 19, 2024