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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 4076 - 4100 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:9352 type 2 diabetes mellitus WB:WBGene00020921 Caenorhabditis elegans 180836 W01C8.5
  • MGI:6194238
DOID:9074 systemic lupus erythematosus WB:WBGene00020921 Caenorhabditis elegans 180836 W01C8.5
  • MGI:6194238
DOID:11247 disseminated intravascular coagulation WB:WBGene00020921 Caenorhabditis elegans 180836 W01C8.5
  • MGI:6194238
DOID:3410 carotid artery thrombosis WB:WBGene00020921 Caenorhabditis elegans 180836 W01C8.5
  • MGI:6194238
DOID:326 ischemia WB:WBGene00020921 Caenorhabditis elegans 180836 W01C8.5
  • MGI:6194238
DOID:10223 dermatomyositis WB:WBGene00020921 Caenorhabditis elegans 180836 W01C8.5
  • MGI:6194238
DOID:3393 coronary artery disease WB:WBGene00020921 Caenorhabditis elegans 180836 W01C8.5
  • MGI:6194238
DOID:8577 ulcerative colitis WB:WBGene00020921 Caenorhabditis elegans 180836 W01C8.5
  • MGI:6194238
DOID:3021 acute kidney failure WB:WBGene00020921 Caenorhabditis elegans 180836 W01C8.5
  • MGI:6194238
DOID:7147 ankylosing spondylitis WB:WBGene00020921 Caenorhabditis elegans 180836 W01C8.5
  • MGI:6194238
DOID:2452 thrombophilia WB:WBGene00020921 Caenorhabditis elegans 180836 W01C8.5
  • MGI:6194238
DOID:783 end stage renal disease WB:WBGene00020921 Caenorhabditis elegans 180836 W01C8.5
  • MGI:6194238
DOID:0111908 thrombophilia due to thrombomodulin defect WB:WBGene00020921 Caenorhabditis elegans 180836 W01C8.5
  • MGI:6194238
DOID:0080301 atypical hemolytic-uremic syndrome WB:WBGene00020921 Caenorhabditis elegans 180836 W01C8.5
  • MGI:6194238
DOID:0112313 brain small vessel disease WB:WBGene00020921 Caenorhabditis elegans 180836 W01C8.5
  • MGI:6194238
DOID:2945 severe acute respiratory syndrome WB:WBGene00020921 Caenorhabditis elegans 180836 W01C8.5
  • MGI:6194238
DOID:2841 asthma WB:WBGene00020921 Caenorhabditis elegans 180836 W01C8.5
  • MGI:6194238
DOID:1459 hypothyroidism WB:WBGene00020921 Caenorhabditis elegans 180836 W01C8.5
  • MGI:6194238
DOID:10652 Alzheimer's disease WB:WBGene00020921 Caenorhabditis elegans 180836 W01C8.5
  • MGI:6194238
DOID:13809 familial combined hyperlipidemia WB:WBGene00020921 Caenorhabditis elegans 180836 W01C8.5
  • MGI:6194238
DOID:0050156 idiopathic pulmonary fibrosis WB:WBGene00020921 Caenorhabditis elegans 180836 W01C8.5
  • MGI:6194238
DOID:5212 congenital disorder of glycosylation WB:WBGene00020820 Caenorhabditis elegans 175920 algn-1
  • MGI:6194238
DOID:0080563 congenital disorder of glycosylation Ik WB:WBGene00020820 Caenorhabditis elegans 175920 algn-1
  • MGI:6194238
DOID:0050570 congenital disorder of glycosylation type I WB:WBGene00020820 Caenorhabditis elegans 175920 algn-1
  • MGI:6194238
DOID:0111974 immunodeficiency 59 WB:WBGene00020781 Caenorhabditis elegans 174033 T24H7.2
  • 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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