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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 October 9, 2024
Displaying entries 69926 - 69950 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:2394 ovarian cancer HGNC:603 Homo sapiens (human) 338 APOB
  • PMID:9023386
DOID:8947 diabetic retinopathy HGNC:603 Homo sapiens (human) 338 APOB
  • PMID:19448981
DOID:4606 bile duct cancer HGNC:603 Homo sapiens (human) 338 APOB
  • PMID:18296645
DOID:9744 type 1 diabetes mellitus HGNC:603 Homo sapiens (human) 338 APOB
  • PMID:1579407
  • PMID:19171731
DOID:1184 nephrotic syndrome HGNC:603 Homo sapiens (human) 338 APOB
  • MGI:6194238
DOID:0111061 familial hypobetalipoproteinemia 2 HGNC:603 Homo sapiens (human) 338 APOB
  • MGI:6194238
DOID:1168 familial hyperlipidemia HGNC:603 Homo sapiens (human) 338 APOB
  • PMID:7627691
DOID:1712 aortic valve stenosis HGNC:603 Homo sapiens (human) 338 APOB
  • PMID:11903341
DOID:9452 steatotic liver disease HGNC:603 Homo sapiens (human) 338 APOB
  • MGI:6194238
DOID:12241 beta thalassemia HGNC:603 Homo sapiens (human) 338 APOB
  • PMID:9180253
DOID:10923 sickle cell anemia HGNC:603 Homo sapiens (human) 338 APOB
  • PMID:24035168
DOID:3526 cerebral infarction HGNC:603 Homo sapiens (human) 338 APOB
  • PMID:2352345
DOID:3393 coronary artery disease HGNC:603 Homo sapiens (human) 338 APOB
  • PMID:1732399
  • PMID:28167353
  • PMID:9585673
DOID:2349 arteriosclerosis HGNC:603 Homo sapiens (human) 338 APOB
  • PMID:19260948
DOID:4607 biliary tract cancer HGNC:603 Homo sapiens (human) 338 APOB
  • PMID:18076041
DOID:3121 gallbladder cancer HGNC:603 Homo sapiens (human) 338 APOB
  • PMID:17696941
  • PMID:20082485
DOID:1287 cardiovascular system disease HGNC:603 Homo sapiens (human) 338 APOB
  • PMID:27578115
DOID:13809 familial combined hyperlipidemia HGNC:603 Homo sapiens (human) 338 APOB
  • PMID:16797745
DOID:13810 familial hypercholesterolemia HGNC:603 Homo sapiens (human) 338 APOB
  • PMID:3627182
  • PMID:9603795
  • RGD:7240710
DOID:0111062 familial hypobetalipoproteinemia 1 HGNC:603 Homo sapiens (human) 338 APOB
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus HGNC:603 Homo sapiens (human) 338 APOB
  • PMID:15161783
  • PMID:18945923
DOID:1390 hypobetalipoproteinemia HGNC:603 Homo sapiens (human) 338 APOB
  • PMID:16728468
  • PMID:3473077
DOID:4608 common bile duct neoplasm HGNC:603 Homo sapiens (human) 338 APOB
  • PMID:18076041
DOID:9970 obesity HGNC:603 Homo sapiens (human) 338 APOB
  • PMID:16752182
DOID:9351 diabetes mellitus HGNC:603 Homo sapiens (human) 338 APOB
  • PMID:2352345

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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: December 9, 2024