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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 3251 - 3275 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▲ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
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: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:0081243 rhizomelic chondrodysplasia punctate type 4 HGNC:26222 Homo sapiens (human) 84188 FAR1
  • RGD:7240710
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:10908 hydrocephalus HGNC:26267 Homo sapiens (human) 84197 POMK
  • MGI:6194238
DOID:0111235 congenital muscular dystrophy-dystroglycanopathy type A12 HGNC:26267 Homo sapiens (human) 84197 POMK
  • RGD:7240710
DOID:0112381 muscular dystrophy-dystroglycanopathy type C12 HGNC:26267 Homo sapiens (human) 84197 POMK
  • RGD:7240710
DOID:10588 adrenoleukodystrophy HGNC:26292 Homo sapiens (human) 79993 ELOVL7
  • MGI:6194238
DOID:12689 acoustic neuroma HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • PMID:12540498
DOID:219 colon cancer HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • MGI:6194238
DOID:1574 alcohol use disorder HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • MGI:6194238
  • PMID:29404485
DOID:11981 morbid obesity HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • PMID:12883487
DOID:9452 steatotic liver disease HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • MGI:6194238
  • PMID:14606109
DOID:9744 type 1 diabetes mellitus HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • PMID:12743671

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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