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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 9776 - 9800 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:0080208 metabolic dysfunction-associated steatotic liver disease SGD:S000005771 Saccharomyces cerevisiae S288C 854419 DGA1
  • MGI:6194238
DOID:9970 obesity HGNC:20113 Homo sapiens (human) 123099 DEGS2
  • MGI:6194238
DOID:1289 neurodegenerative disease HGNC:20113 Homo sapiens (human) 123099 DEGS2
  • MGI:6194238
DOID:0070399 hypomyelinating leukodystrophy 18 HGNC:13709 Homo sapiens (human) 8560 DEGS1
  • RGD:7240710
DOID:9970 obesity HGNC:13709 Homo sapiens (human) 8560 DEGS1
  • MGI:6194238
DOID:1289 neurodegenerative disease HGNC:13709 Homo sapiens (human) 8560 DEGS1
  • MGI:6194238
DOID:0060786 hypomyelinating leukodystrophy HGNC:13709 Homo sapiens (human) 8560 DEGS1
  • MGI:6194238
DOID:0080569 congenital disorder of glycosylation Ir HGNC:2728 Homo sapiens (human) 1650 DDOST
  • RGD:7240710
DOID:0111258 pentosuria HGNC:18985 Homo sapiens (human) 51181 DCXR
  • RGD:7240710
DOID:5844 myocardial infarction HGNC:2705 Homo sapiens (human) 1634 DCN
  • MGI:6194238
DOID:0060445 congenital stromal corneal dystrophy HGNC:2705 Homo sapiens (human) 1634 DCN
  • RGD:7240710
DOID:13359 Ehlers-Danlos syndrome HGNC:2705 Homo sapiens (human) 1634 DCN
  • MGI:6194238
DOID:3459 breast carcinoma HGNC:2705 Homo sapiens (human) 1634 DCN
  • PMID:18688028
DOID:9970 obesity HGNC:2705 Homo sapiens (human) 1634 DCN
  • MGI:6194238
DOID:3070 high grade glioma HGNC:2705 Homo sapiens (human) 1634 DCN
  • PMID:15475879
DOID:2841 asthma HGNC:2705 Homo sapiens (human) 1634 DCN
  • MGI:6194238
DOID:11714 gestational diabetes HGNC:2705 Homo sapiens (human) 1634 DCN
  • PMID:16630654
DOID:9352 type 2 diabetes mellitus HGNC:2705 Homo sapiens (human) 1634 DCN
  • PMID:18414424
DOID:9269 maple syrup urine disease HGNC:2698 Homo sapiens (human) 1629 DBT
  • MGI:6194238
DOID:0111232 congenital muscular dystrophy-dystroglycanopathy type A9 HGNC:2666 Homo sapiens (human) 1605 DAG1
  • RGD:7240710
DOID:0050453 lissencephaly HGNC:2666 Homo sapiens (human) 1605 DAG1
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus HGNC:2666 Homo sapiens (human) 1605 DAG1
  • MGI:6194238
DOID:11723 Duchenne muscular dystrophy HGNC:2666 Homo sapiens (human) 1605 DAG1
  • PMID:11445638
  • PMID:15833425
  • PMID:7630355
DOID:12236 primary biliary cholangitis HGNC:2666 Homo sapiens (human) 1605 DAG1
  • MGI:6194238
DOID:0050559 Fukuyama congenital muscular dystrophy HGNC:2666 Homo sapiens (human) 1605 DAG1
  • PMID:11445638

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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