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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 63601 - 63625 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:6432 pulmonary hypertension HGNC:11935 Homo sapiens (human) 959 CD40LG
  • MGI:6194238
DOID:783 end stage renal disease HGNC:11935 Homo sapiens (human) 959 CD40LG
  • PMID:19019166
DOID:628 combined T cell and B cell immunodeficiency HGNC:11935 Homo sapiens (human) 959 CD40LG
  • PMID:21543760
DOID:0050589 inflammatory bowel disease HGNC:11935 Homo sapiens (human) 959 CD40LG
  • MGI:6194238
DOID:1485 cystic fibrosis HGNC:11935 Homo sapiens (human) 959 CD40LG
  • PMID:15102009
DOID:1168 familial hyperlipidemia HGNC:11935 Homo sapiens (human) 959 CD40LG
  • PMID:21485068
DOID:12449 aplastic anemia HGNC:11935 Homo sapiens (human) 959 CD40LG
  • PMID:22537155
DOID:0060022 CD40 ligand deficiency HGNC:11935 Homo sapiens (human) 959 CD40LG
  • PMID:15358621
  • PMID:16508335
  • PMID:17553565
  • PMID:21841160
  • RGD:7240710
DOID:526 human immunodeficiency virus infectious disease HGNC:11935 Homo sapiens (human) 959 CD40LG
  • PMID:21177803
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

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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