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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 63626 - 63650 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
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
DOID:3407 carotid artery disease HGNC:11935 Homo sapiens (human) 959 CD40LG
  • PMID:15817881
  • PMID:16752185
DOID:11713 diabetic angiopathy HGNC:11935 Homo sapiens (human) 959 CD40LG
  • PMID:14963650
DOID:10923 sickle cell anemia HGNC:11935 Homo sapiens (human) 959 CD40LG
  • PMID:24368019
DOID:9744 type 1 diabetes mellitus HGNC:11935 Homo sapiens (human) 959 CD40LG
  • MGI:6194238
  • PMID:16505242
DOID:9201 lichen planus HGNC:11935 Homo sapiens (human) 959 CD40LG
  • PMID:18050371
DOID:13241 Behcet's disease HGNC:11935 Homo sapiens (human) 959 CD40LG
  • PMID:22116092
DOID:12361 Graves' disease HGNC:11935 Homo sapiens (human) 959 CD40LG
  • PMID:8875745
DOID:0080162 lupus nephritis HGNC:11935 Homo sapiens (human) 959 CD40LG
  • PMID:12632425
  • PMID:15693003
  • PMID:20726330
DOID:3744 cervical squamous cell carcinoma HGNC:11934 Homo sapiens (human) 7292 TNFSF4
  • PMID:28086903
DOID:14557 primary pulmonary hypertension HGNC:11934 Homo sapiens (human) 7292 TNFSF4
  • MGI:6194238
DOID:5844 myocardial infarction HGNC:11934 Homo sapiens (human) 7292 TNFSF4
  • PMID:15750594
  • RGD:7240710
DOID:9744 type 1 diabetes mellitus HGNC:11934 Homo sapiens (human) 7292 TNFSF4
  • MGI:6194238
DOID:0110896 inflammatory bowel disease 16 HGNC:11931 Homo sapiens (human) 9966 TNFSF15
  • MGI:6194238
DOID:2986 IgA glomerulonephritis HGNC:11930 Homo sapiens (human) 8740 TNFSF14
  • MGI:6194238
DOID:2986 IgA glomerulonephritis HGNC:11929 Homo sapiens (human) 10673 TNFSF13B
  • MGI:6194238
DOID:12894 Sjogren's syndrome HGNC:11929 Homo sapiens (human) 10673 TNFSF13B
  • MGI:6194238

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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: December 9, 2024