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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 11026 - 11050 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▲ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0050559 Fukuyama congenital muscular dystrophy WB:WBGene00020924 Caenorhabditis elegans 189104 W02B3.4
  • MGI:6194238
DOID:0110296 autosomal recessive limb-girdle muscular dystrophy type 2M WB:WBGene00020924 Caenorhabditis elegans 189104 W02B3.4
  • MGI:6194238
DOID:0110443 dilated cardiomyopathy 1B WB:WBGene00020924 Caenorhabditis elegans 189104 W02B3.4
  • MGI:6194238
DOID:0050588 muscular dystrophy-dystroglycanopathy type B1 WB:WBGene00020924 Caenorhabditis elegans 189104 W02B3.4
  • MGI:6194238
DOID:0110960 Gaucher's disease perinatal lethal WB:WBGene00021160 Caenorhabditis elegans 177314 gba-4
  • MGI:6194238
DOID:0112250 Gaucher's disease type IIIC WB:WBGene00021160 Caenorhabditis elegans 177314 gba-4
  • MGI:6194238
DOID:0110957 Gaucher's disease type I WB:WBGene00021160 Caenorhabditis elegans 177314 gba-4
  • MGI:6194238
DOID:0050474 Netherton syndrome WB:WBGene00021160 Caenorhabditis elegans 177314 gba-4
  • MGI:6194238
DOID:1926 Gaucher's disease WB:WBGene00021160 Caenorhabditis elegans 177314 gba-4
  • MGI:6194238
DOID:0080855 Parkinsonism WB:WBGene00021160 Caenorhabditis elegans 177314 gba-4
  • MGI:6194238
DOID:0110958 Gaucher's disease type II WB:WBGene00021160 Caenorhabditis elegans 177314 gba-4
  • MGI:6194238
DOID:8893 psoriasis WB:WBGene00021160 Caenorhabditis elegans 177314 gba-4
  • MGI:6194238
DOID:14330 Parkinson's disease WB:WBGene00021160 Caenorhabditis elegans 177314 gba-4
  • MGI:6194238
DOID:0110959 Gaucher's disease type III WB:WBGene00021160 Caenorhabditis elegans 177314 gba-4
  • MGI:6194238
DOID:0060892 late onset Parkinson's disease WB:WBGene00021160 Caenorhabditis elegans 177314 gba-4
  • MGI:6194238
DOID:12217 Lewy body dementia WB:WBGene00021160 Caenorhabditis elegans 177314 gba-4
  • MGI:6194238
DOID:0050570 congenital disorder of glycosylation type I WB:WBGene00022044 Caenorhabditis elegans 176874 dpm-1
  • MGI:6194238
DOID:0080557 congenital disorder of glycosylation Ie WB:WBGene00022044 Caenorhabditis elegans 176874 dpm-1
  • MGI:6194238
DOID:2747 glycogen storage disease WB:WBGene00022199 Caenorhabditis elegans 180583 pfk-1.1
  • MGI:6194238
DOID:11721 glycogen storage disease VII WB:WBGene00022199 Caenorhabditis elegans 180583 pfk-1.1
  • MGI:6194238
DOID:0014667 disease of metabolism WB:WBGene00022199 Caenorhabditis elegans 180583 pfk-1.1
  • MGI:6194238
DOID:0080201 Peters plus syndrome WB:WBGene00022576 Caenorhabditis elegans 178968 ZC250.2
  • MGI:6194238
DOID:0050570 congenital disorder of glycosylation type I WB:WBGene00022629 Caenorhabditis elegans 179185 algn-12
  • MGI:6194238
DOID:0080559 congenital disorder of glycosylation Ig WB:WBGene00022629 Caenorhabditis elegans 179185 algn-12
  • MGI:6194238
DOID:3525 middle cerebral artery infarction WB:WBGene00022817 Caenorhabditis elegans 176077 upp-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