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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 10976 - 11000 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▲ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:1380 endometrial cancer WB:WBGene00018206 Caenorhabditis elegans 185500 ugt-61
  • MGI:6194238
DOID:2043 hepatitis B WB:WBGene00018206 Caenorhabditis elegans 185500 ugt-61
  • MGI:6194238
DOID:3803 Crigler-Najjar syndrome WB:WBGene00018206 Caenorhabditis elegans 185500 ugt-61
  • MGI:6194238
DOID:2739 Gilbert syndrome WB:WBGene00018206 Caenorhabditis elegans 185500 ugt-61
  • MGI:6194238
DOID:1793 pancreatic cancer WB:WBGene00018206 Caenorhabditis elegans 185500 ugt-61
  • MGI:6194238
DOID:2741 bilirubin metabolic disorder WB:WBGene00018206 Caenorhabditis elegans 185500 ugt-61
  • MGI:6194238
DOID:8692 myeloid leukemia WB:WBGene00018206 Caenorhabditis elegans 185500 ugt-61
  • MGI:6194238
DOID:11151 cholecystolithiasis WB:WBGene00018206 Caenorhabditis elegans 185500 ugt-61
  • MGI:6194238
DOID:10763 hypertension WB:WBGene00019127 Caenorhabditis elegans 174001 cgt-3
  • MGI:6194238
DOID:0050570 congenital disorder of glycosylation type I WB:WBGene00019276 Caenorhabditis elegans 178822 algn-5
  • MGI:6194238
DOID:0080322 polycystic kidney disease WB:WBGene00019276 Caenorhabditis elegans 178822 algn-5
  • MGI:6194238
DOID:2018 hyperinsulinism WB:WBGene00019295 Caenorhabditis elegans 177363 pfkb-1.2
  • MGI:6194238
DOID:0110658 congenital myasthenic syndrome 15 WB:WBGene00019725 Caenorhabditis elegans 187398 algn-14
  • MGI:6194238
DOID:0060363 glycerol kinase deficiency WB:WBGene00020007 Caenorhabditis elegans 173747 R11F4.1
  • MGI:6194238
DOID:13810 familial hypercholesterolemia WB:WBGene00020007 Caenorhabditis elegans 173747 R11F4.1
  • MGI:6194238
DOID:653 purine-pyrimidine metabolic disorder WB:WBGene00020036 Caenorhabditis elegans 172008 R12E2.11
  • MGI:6194238
DOID:0050833 orotic aciduria WB:WBGene00020036 Caenorhabditis elegans 172008 R12E2.11
  • MGI:6194238
DOID:162 cancer WB:WBGene00020185 Caenorhabditis elegans 171965 pgk-1
  • MGI:6194238
DOID:14330 Parkinson's disease WB:WBGene00020185 Caenorhabditis elegans 171965 pgk-1
  • MGI:6194238
DOID:583 hemolytic anemia WB:WBGene00020185 Caenorhabditis elegans 171965 pgk-1
  • MGI:6194238
DOID:0111933 phosphoglycerate kinase 1 deficiency WB:WBGene00020185 Caenorhabditis elegans 171965 pgk-1
  • MGI:6194238
DOID:1508 candidiasis WB:WBGene00020222 Caenorhabditis elegans 188084 fut-6
  • MGI:6194238
DOID:0050559 Fukuyama congenital muscular dystrophy WB:WBGene00020307 Caenorhabditis elegans 173469 T07D3.4
  • MGI:6194238
DOID:0050588 muscular dystrophy-dystroglycanopathy type B1 WB:WBGene00020307 Caenorhabditis elegans 173469 T07D3.4
  • MGI:6194238
DOID:0110443 dilated cardiomyopathy 1B WB:WBGene00020307 Caenorhabditis elegans 173469 T07D3.4
  • 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