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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 1801 - 1825 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:14500 fucosidosis WB:WBGene00012225 Caenorhabditis elegans 189173 W03G11.3
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus WB:WBGene00012225 Caenorhabditis elegans 189173 W03G11.3
  • MGI:6194238
DOID:9744 type 1 diabetes mellitus WB:WBGene00012225 Caenorhabditis elegans 189173 W03G11.3
  • MGI:6194238
DOID:8947 diabetic retinopathy WB:WBGene00012225 Caenorhabditis elegans 189173 W03G11.3
  • MGI:6194238
DOID:9351 diabetes mellitus WB:WBGene00012225 Caenorhabditis elegans 189173 W03G11.3
  • MGI:6194238
DOID:0110284 autosomal recessive limb-girdle muscular dystrophy type 2L WB:WBGene00020924 Caenorhabditis elegans 189104 W02B3.4
  • MGI:6194238
DOID:0112379 muscular dystrophy-dystroglycanopathy type B4 WB:WBGene00020924 Caenorhabditis elegans 189104 W02B3.4
  • MGI:6194238
DOID:9884 muscular dystrophy WB:WBGene00020924 Caenorhabditis elegans 189104 W02B3.4
  • MGI:6194238
DOID:0110444 dilated cardiomyopathy 1X WB:WBGene00020924 Caenorhabditis elegans 189104 W02B3.4
  • MGI:6194238
DOID:0050560 Walker-Warburg syndrome WB:WBGene00020924 Caenorhabditis elegans 189104 W02B3.4
  • MGI:6194238
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:3498 pancreatic ductal adenocarcinoma HGNC:12705 Homo sapiens (human) 8876 VNN1
  • PMID:32663515
DOID:5844 myocardial infarction HGNC:2464 Homo sapiens (human) 1462 VCAN
  • MGI:6194238
DOID:10941 intracranial aneurysm HGNC:2464 Homo sapiens (human) 1462 VCAN
  • PMID:16917090
DOID:8481 rheumatic myocarditis HGNC:12663 Homo sapiens (human) 7412 VCAM1
  • PMID:22987107
DOID:1793 pancreatic cancer HGNC:12663 Homo sapiens (human) 7412 VCAM1
  • PMID:17652277
DOID:10763 hypertension HGNC:12663 Homo sapiens (human) 7412 VCAM1
  • MGI:6194238
  • PMID:20569722
DOID:2355 anemia HGNC:12663 Homo sapiens (human) 7412 VCAM1
  • PMID:18974656
DOID:5082 liver cirrhosis HGNC:12663 Homo sapiens (human) 7412 VCAM1
  • MGI:6194238
DOID:12918 thromboangiitis obliterans HGNC:12663 Homo sapiens (human) 7412 VCAM1
  • MGI:6194238
  • PMID:12086338
DOID:1168 familial hyperlipidemia HGNC:12663 Homo sapiens (human) 7412 VCAM1
  • MGI:6194238
DOID:4989 pancreatitis HGNC:12663 Homo sapiens (human) 7412 VCAM1
  • PMID:12923961

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

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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