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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 1476 - 1500 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▼ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:1793 pancreatic cancer MGI:2135738 Mus musculus (house mouse) 80908 Abo
  • MGI:6194238
DOID:2237 hepatitis MGI:2135738 Mus musculus (house mouse) 80908 Abo
  • MGI:6194238
DOID:9952 acute lymphoblastic leukemia MGI:2135738 Mus musculus (house mouse) 80908 Abo
  • MGI:6194238
DOID:0080600 COVID-19 MGI:2135738 Mus musculus (house mouse) 80908 Abo
  • MGI:6194238
DOID:1240 leukemia MGI:2135738 Mus musculus (house mouse) 80908 Abo
  • MGI:6194238
DOID:4948 gallbladder carcinoma MGI:2135738 Mus musculus (house mouse) 80908 Abo
  • MGI:6194238
DOID:2945 severe acute respiratory syndrome MGI:2135738 Mus musculus (house mouse) 80908 Abo
  • MGI:6194238
DOID:0081267 graft-versus-host disease MGI:2135738 Mus musculus (house mouse) 80908 Abo
  • MGI:6194238
DOID:14067 Plasmodium falciparum malaria MGI:2135738 Mus musculus (house mouse) 80908 Abo
  • MGI:6194238
DOID:10763 hypertension MGI:2135738 Mus musculus (house mouse) 80908 Abo
  • MGI:6194238
DOID:423 myopathy HGNC:16781 Homo sapiens (human) 80896 NPL
  • MGI:6194238
DOID:1115 sarcoma HGNC:21350 Homo sapiens (human) 8050 PDHX
  • PMID:31089155
DOID:3649 pyruvate decarboxylase deficiency HGNC:21350 Homo sapiens (human) 8050 PDHX
  • RGD:7240710
DOID:1459 hypothyroidism HGNC:18590 Homo sapiens (human) 80339 PNPLA3
  • MGI:6194238
DOID:3393 coronary artery disease HGNC:18590 Homo sapiens (human) 80339 PNPLA3
  • PMID:31377187
DOID:9352 type 2 diabetes mellitus HGNC:18590 Homo sapiens (human) 80339 PNPLA3
  • PMID:31377187
DOID:9970 obesity HGNC:18590 Homo sapiens (human) 80339 PNPLA3
  • MGI:6194238
DOID:0050729 Chanarin-Dorfman syndrome HGNC:18590 Homo sapiens (human) 80339 PNPLA3
  • MGI:6194238
DOID:0060158 acquired metabolic disease HGNC:18590 Homo sapiens (human) 80339 PNPLA3
  • MGI:6194238
DOID:5082 liver cirrhosis HGNC:18590 Homo sapiens (human) 80339 PNPLA3
  • PMID:20648474
  • PMID:29674183
  • PMID:31377187
DOID:9452 steatotic liver disease HGNC:18590 Homo sapiens (human) 80339 PNPLA3
  • PMID:21319195
  • PMID:23564580
  • PMID:25284145
  • PMID:25678388
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:18590 Homo sapiens (human) 80339 PNPLA3
  • MGI:6194238
  • PMID:24477042
  • PMID:24831885
  • PMID:26740948
DOID:684 hepatocellular carcinoma HGNC:18590 Homo sapiens (human) 80339 PNPLA3
  • PMID:21319195
DOID:14250 Down syndrome MGI:1916863 Mus musculus (house mouse) 80294 Pofut2
  • MGI:6194238
DOID:9256 colorectal cancer HGNC:14897 Homo sapiens (human) 80271 ITPKC
  • PMID:33470690

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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