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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 10626 - 10650 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▼ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:4195 hyperglycemia HGNC:2623 Homo sapiens (human) 1559 CYP2C9
  • PMID:17597710
DOID:6432 pulmonary hypertension MGI:1196334 Mus musculus (house mouse) 15587 Hyal2
  • MGI:6194238
DOID:12798 mucopolysaccharidosis MGI:96298 Mus musculus (house mouse) 15586 Hyal1
  • MGI:6194238
DOID:0050809 mucopolysaccharidosis IX MGI:96298 Mus musculus (house mouse) 15586 Hyal1
  • MGI:6194238
  • PMID:18344557
DOID:6432 pulmonary hypertension MGI:96298 Mus musculus (house mouse) 15586 Hyal1
  • MGI:6194238
DOID:1073 renal hypertension HGNC:2622 Homo sapiens (human) 1558 CYP2C8
  • PMID:20495177
DOID:9352 type 2 diabetes mellitus HGNC:2622 Homo sapiens (human) 1558 CYP2C8
  • MGI:6194238
DOID:783 end stage renal disease HGNC:2622 Homo sapiens (human) 1558 CYP2C8
  • PMID:18769365
DOID:0050073 invasive aspergillosis HGNC:2621 Homo sapiens (human) 1557 CYP2C19
  • PMID:26861072
DOID:0050083 Keshan disease HGNC:2621 Homo sapiens (human) 1557 CYP2C19
  • PMID:26893848
DOID:1612 breast cancer HGNC:2621 Homo sapiens (human) 1557 CYP2C19
  • PMID:26799162
DOID:750 peptic ulcer disease HGNC:2621 Homo sapiens (human) 1557 CYP2C19
  • PMID:23267857
  • PMID:9867757
DOID:399 tuberculosis HGNC:2621 Homo sapiens (human) 1557 CYP2C19
  • PMID:27393733
DOID:5520 head and neck squamous cell carcinoma HGNC:2621 Homo sapiens (human) 1557 CYP2C19
  • PMID:19954746
DOID:9538 multiple myeloma HGNC:2621 Homo sapiens (human) 1557 CYP2C19
  • PMID:17666363
  • PMID:20684753
DOID:684 hepatocellular carcinoma HGNC:2621 Homo sapiens (human) 1557 CYP2C19
  • PMID:11021356
DOID:9352 type 2 diabetes mellitus HGNC:2621 Homo sapiens (human) 1557 CYP2C19
  • MGI:6194238
DOID:4661 multiple chemical sensitivity HGNC:2621 Homo sapiens (human) 1557 CYP2C19
  • PMID:23936614
DOID:14067 Plasmodium falciparum malaria HGNC:2621 Homo sapiens (human) 1557 CYP2C19
  • PMID:10471063
DOID:10923 sickle cell anemia HGNC:2621 Homo sapiens (human) 1557 CYP2C19
  • PMID:20831548
DOID:12930 dilated cardiomyopathy HGNC:2621 Homo sapiens (human) 1557 CYP2C19
  • PMID:26893848
DOID:9976 heroin dependence HGNC:2621 Homo sapiens (human) 1557 CYP2C19
  • PMID:24016178
  • PMID:24956251
DOID:13922 eosinophilic esophagitis HGNC:2621 Homo sapiens (human) 1557 CYP2C19
  • PMID:26416193
DOID:9452 steatotic liver disease MGI:109521 Mus musculus (house mouse) 15558 Htr2a
  • MGI:6194238
DOID:8689 anorexia nervosa MGI:109521 Mus musculus (house mouse) 15558 Htr2a
  • 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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Last updated: August 19, 2024