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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 1001 - 1025 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:418 systemic scleroderma MGI:1340899 Mus musculus (house mouse) 12654 Chi3l1
  • MGI:6194238
DOID:0080199 colorectal carcinoma MGI:1340899 Mus musculus (house mouse) 12654 Chi3l1
  • MGI:6194238
DOID:6000 congestive heart failure MGI:1340899 Mus musculus (house mouse) 12654 Chi3l1
  • MGI:6194238
DOID:5844 myocardial infarction MGI:1340899 Mus musculus (house mouse) 12654 Chi3l1
  • MGI:6194238
DOID:10591 pre-eclampsia MGI:1340899 Mus musculus (house mouse) 12654 Chi3l1
  • MGI:6194238
DOID:9744 type 1 diabetes mellitus MGI:1340899 Mus musculus (house mouse) 12654 Chi3l1
  • MGI:6194238
DOID:0050127 sinusitis MGI:1330860 Mus musculus (house mouse) 12655 Chil3
  • MGI:6194238
DOID:2841 asthma MGI:1330860 Mus musculus (house mouse) 12655 Chil3
  • MGI:6194238
DOID:0112198 spondyloepimetaphyseal dysplasia with joint laxity type 1 HGNC:17978 Homo sapiens (human) 126792 B3GALT6
  • RGD:7240710
DOID:0050802 Ehlers-Danlos syndrome spondylodysplastic type 2 HGNC:17978 Homo sapiens (human) 126792 B3GALT6
  • RGD:7240710
DOID:13359 Ehlers-Danlos syndrome HGNC:17978 Homo sapiens (human) 126792 B3GALT6
  • MGI:6194238
DOID:0050741 alcohol dependence HGNC:252 Homo sapiens (human) 127 ADH4
  • PMID:20077761
DOID:0080101 Compton-North congenital myopathy HGNC:2171 Homo sapiens (human) 1272 CNTN1
  • MGI:6194238
  • RGD:7240710
DOID:2841 asthma HGNC:253 Homo sapiens (human) 128 ADH5
  • PMID:17543375
  • PMID:19395503
  • PMID:19514054
DOID:0080952 AMED syndrome HGNC:253 Homo sapiens (human) 128 ADH5
  • RGD:7240710
DOID:1574 alcohol use disorder HGNC:253 Homo sapiens (human) 128 ADH5
  • MGI:6194238
DOID:13580 cholestasis HGNC:253 Homo sapiens (human) 128 ADH5
  • MGI:6194238
DOID:9884 muscular dystrophy MGI:88459 Mus musculus (house mouse) 12833 Col6a1
  • MGI:6194238
DOID:0050663 Bethlem myopathy MGI:88459 Mus musculus (house mouse) 12833 Col6a1
  • MGI:6194238
  • PMID:14625552
  • PMID:9817932
DOID:0050558 Ullrich congenital muscular dystrophy MGI:88459 Mus musculus (house mouse) 12833 Col6a1
  • MGI:6194238
  • PMID:28043812
DOID:0050557 congenital muscular dystrophy MGI:88459 Mus musculus (house mouse) 12833 Col6a1
  • MGI:6194238
DOID:12399 pathological gambling MGI:88470 Mus musculus (house mouse) 12846 Comt
  • MGI:6194238
DOID:13078 eumycotic mycetoma MGI:88470 Mus musculus (house mouse) 12846 Comt
  • MGI:6194238
DOID:2394 ovarian cancer MGI:88470 Mus musculus (house mouse) 12846 Comt
  • MGI:6194238
DOID:0060041 autism spectrum disorder MGI:88470 Mus musculus (house mouse) 12846 Comt
  • MGI:6194238

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

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