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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 10151 - 10175 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:10320 asbestosis HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • PMID:20514434
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • MGI:6194238
DOID:9970 obesity HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • MGI:6194238
DOID:0050868 hepatocellular adenoma HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • MGI:6194238
DOID:3083 chronic obstructive pulmonary disease HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • PMID:17442289
DOID:10534 stomach cancer HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • PMID:22957075
DOID:1596 depressive disorder HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • MGI:6194238
DOID:2841 asthma HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • PMID:20514434
DOID:552 pneumonia HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • PMID:15928955
DOID:0050866 oral squamous cell carcinoma HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • PMID:22954124
DOID:3525 middle cerebral artery infarction HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • MGI:6194238
DOID:5520 head and neck squamous cell carcinoma HGNC:2623 Homo sapiens (human) 1559 CYP2C9
  • PMID:19954746
DOID:11054 urinary bladder cancer HGNC:2623 Homo sapiens (human) 1559 CYP2C9
  • PMID:16985032
DOID:0080665 warfarin resistance HGNC:2623 Homo sapiens (human) 1559 CYP2C9
  • RGD:7240710
DOID:9351 diabetes mellitus HGNC:2623 Homo sapiens (human) 1559 CYP2C9
  • PMID:16303885
  • PMID:16788382
DOID:10763 hypertension HGNC:2623 Homo sapiens (human) 1559 CYP2C9
  • PMID:17305793
  • PMID:19669737
DOID:9993 hypoglycemia HGNC:2623 Homo sapiens (human) 1559 CYP2C9
  • PMID:15963101
DOID:9352 type 2 diabetes mellitus HGNC:2623 Homo sapiens (human) 1559 CYP2C9
  • PMID:16325295
DOID:4195 hyperglycemia HGNC:2623 Homo sapiens (human) 1559 CYP2C9
  • PMID:17597710
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

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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