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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 70951 - 70975 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▲ FlyGlycoDB Evidence Code Names References
DOID:9256 colorectal cancer WB:WBGene00006776 Caenorhabditis elegans 172233 unc-40
  • MGI:6194238
DOID:3748 esophagus squamous cell carcinoma WB:WBGene00006776 Caenorhabditis elegans 172233 unc-40
  • MGI:6194238
DOID:0111153 congenital mirror movement disorder WB:WBGene00006776 Caenorhabditis elegans 172233 unc-40
  • MGI:6194238
DOID:0112202 developmental and epileptic encephalopathy WB:WBGene00006783 Caenorhabditis elegans 176431 unc-47
  • MGI:6194238
DOID:0060170 generalized epilepsy with febrile seizures plus WB:WBGene00006783 Caenorhabditis elegans 176431 unc-47
  • MGI:6194238
DOID:3328 temporal lobe epilepsy WB:WBGene00006783 Caenorhabditis elegans 176431 unc-47
  • MGI:6194238
DOID:1574 alcohol use disorder WB:WBGene00006783 Caenorhabditis elegans 176431 unc-47
  • PMID:25342716
DOID:0090005 Schwartz-Jampel syndrome 1 WB:WBGene00006787 Caenorhabditis elegans 175126 unc-52
  • MGI:6194238
DOID:2256 osteochondrodysplasia WB:WBGene00006787 Caenorhabditis elegans 175126 unc-52
  • MGI:6194238
DOID:4195 hyperglycemia WB:WBGene00006787 Caenorhabditis elegans 175126 unc-52
  • MGI:6194238
DOID:0090032 Silverman-Handmaker type dyssegmental dysplasia WB:WBGene00006787 Caenorhabditis elegans 175126 unc-52
  • MGI:6194238
DOID:13481 thanatophoric dysplasia WB:WBGene00006787 Caenorhabditis elegans 175126 unc-52
  • MGI:6194238
DOID:10763 hypertension WB:WBGene00006787 Caenorhabditis elegans 175126 unc-52
  • MGI:6194238
DOID:0060770 dextro-looped transposition of the great arteries WB:WBGene00006787 Caenorhabditis elegans 175126 unc-52
  • MGI:6194238
DOID:3407 carotid artery disease WB:WBGene00006787 Caenorhabditis elegans 175126 unc-52
  • MGI:6194238
DOID:0111153 congenital mirror movement disorder WB:WBGene00006746 Caenorhabditis elegans 180961 unc-6
  • MGI:6194238
DOID:3312 bipolar disorder WB:WBGene00006797 Caenorhabditis elegans 172150 unc-63
  • MGI:6194238
DOID:11832 visual epilepsy WB:WBGene00006797 Caenorhabditis elegans 172150 unc-63
  • MGI:6194238
DOID:0060041 autism spectrum disorder WB:WBGene00006797 Caenorhabditis elegans 172150 unc-63
  • MGI:6194238
DOID:0060682 autosomal dominant nocturnal frontal lobe epilepsy 1 WB:WBGene00006797 Caenorhabditis elegans 172150 unc-63
  • MGI:6194238
DOID:0110679 congenital myasthenic syndrome 4C WB:WBGene00006797 Caenorhabditis elegans 172150 unc-63
  • MGI:6194238
DOID:10652 Alzheimer's disease WB:WBGene00006797 Caenorhabditis elegans 172150 unc-63
  • MGI:6194238
DOID:10534 stomach cancer WB:WBGene00006797 Caenorhabditis elegans 172150 unc-63
  • MGI:6194238
DOID:0050742 nicotine dependence WB:WBGene00006797 Caenorhabditis elegans 172150 unc-63
  • MGI:6194238
DOID:3635 congenital myasthenic syndrome WB:WBGene00006797 Caenorhabditis elegans 172150 unc-63
  • MGI:6194238
  • PMID:20966081

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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: December 9, 2024