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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 71526 - 71550 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:13922 eosinophilic esophagitis HGNC:11935 Homo sapiens (human) 959 CD40LG
  • PMID:21211656
DOID:1936 atherosclerosis HGNC:11935 Homo sapiens (human) 959 CD40LG
  • MGI:6194238
  • PMID:21817131
DOID:9970 obesity HGNC:11935 Homo sapiens (human) 959 CD40LG
  • PMID:20660932
DOID:12894 Sjogren's syndrome HGNC:11935 Homo sapiens (human) 959 CD40LG
  • PMID:12472667
DOID:0070355 overactive bladder syndrome HGNC:11935 Homo sapiens (human) 959 CD40LG
  • PMID:19784793
DOID:0050873 follicular lymphoma HGNC:11935 Homo sapiens (human) 959 CD40LG
  • PMID:25582824
DOID:2988 antiphospholipid syndrome HGNC:11935 Homo sapiens (human) 959 CD40LG
  • PMID:16188945
DOID:8986 narcolepsy HGNC:11935 Homo sapiens (human) 959 CD40LG
  • PMID:21669245
DOID:0050731 vitamin B12 deficiency HGNC:11935 Homo sapiens (human) 959 CD40LG
  • MGI:6194238
DOID:4780 anti-basement membrane glomerulonephritis HGNC:11935 Homo sapiens (human) 959 CD40LG
  • MGI:6194238
DOID:9351 diabetes mellitus HGNC:11935 Homo sapiens (human) 959 CD40LG
  • PMID:17635572
DOID:9074 systemic lupus erythematosus HGNC:11935 Homo sapiens (human) 959 CD40LG
  • MGI:6194238
  • PMID:20726330
DOID:3388 periodontal disease HGNC:11935 Homo sapiens (human) 959 CD40LG
  • MGI:6194238
DOID:5050 Ehrlich tumor carcinoma HGNC:11935 Homo sapiens (human) 959 CD40LG
  • MGI:6194238
DOID:2224 essential thrombocythemia HGNC:11935 Homo sapiens (human) 959 CD40LG
  • PMID:22196954
DOID:9182 pemphigus HGNC:11935 Homo sapiens (human) 959 CD40LG
  • PMID:17531537
DOID:9352 type 2 diabetes mellitus HGNC:11935 Homo sapiens (human) 959 CD40LG
  • PMID:16423632
  • PMID:19280268
DOID:6364 migraine HGNC:11935 Homo sapiens (human) 959 CD40LG
  • PMID:21331754
DOID:0060903 thrombosis HGNC:11935 Homo sapiens (human) 959 CD40LG
  • MGI:6194238
  • PMID:15306157
DOID:6000 congestive heart failure HGNC:11935 Homo sapiens (human) 959 CD40LG
  • PMID:15716285
DOID:4481 allergic rhinitis HGNC:11935 Homo sapiens (human) 959 CD40LG
  • PMID:19086656
DOID:5844 myocardial infarction HGNC:11935 Homo sapiens (human) 959 CD40LG
  • PMID:17635572
DOID:13378 Kawasaki disease HGNC:11935 Homo sapiens (human) 959 CD40LG
  • PMID:12563087
DOID:12132 granulomatosis with polyangiitis HGNC:11935 Homo sapiens (human) 959 CD40LG
  • PMID:21411717
DOID:8677 perinatal necrotizing enterocolitis HGNC:11935 Homo sapiens (human) 959 CD40LG
  • MGI:6194238

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Acknowledgements

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