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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 63776 - 63800 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:14330 Parkinson's disease HGNC:1515 Homo sapiens (human) 831 CAST
  • PMID:10722997
  • PMID:20127884
DOID:0110663 congenital myasthenic syndrome 1A HGNC:1515 Homo sapiens (human) 831 CAST
  • PMID:17853947
DOID:2316 brain ischemia HGNC:1515 Homo sapiens (human) 831 CAST
  • MGI:6194238
DOID:8893 psoriasis HGNC:1515 Homo sapiens (human) 831 CAST
  • PMID:15654835
DOID:9952 acute lymphoblastic leukemia HGNC:1515 Homo sapiens (human) 831 CAST
  • PMID:11264179
DOID:1574 alcohol use disorder HGNC:1515 Homo sapiens (human) 831 CAST
  • MGI:6194238
DOID:14067 Plasmodium falciparum malaria HGNC:1515 Homo sapiens (human) 831 CAST
  • PMID:17359359
DOID:0070526 PLACK syndrome HGNC:1515 Homo sapiens (human) 831 CAST
  • RGD:7240710
DOID:7148 rheumatoid arthritis HGNC:1515 Homo sapiens (human) 831 CAST
  • PMID:7706496
DOID:12894 Sjogren's syndrome HGNC:1515 Homo sapiens (human) 831 CAST
  • PMID:15540513
DOID:10652 Alzheimer's disease HGNC:1515 Homo sapiens (human) 831 CAST
  • PMID:19020018
DOID:9182 pemphigus HGNC:1515 Homo sapiens (human) 831 CAST
  • PMID:16314468
DOID:767 muscular atrophy HGNC:1515 Homo sapiens (human) 831 CAST
  • MGI:6194238
DOID:10763 hypertension HGNC:1515 Homo sapiens (human) 831 CAST
  • MGI:6194238
DOID:9074 systemic lupus erythematosus HGNC:1515 Homo sapiens (human) 831 CAST
  • PMID:12367559
DOID:1936 atherosclerosis HGNC:1514 Homo sapiens (human) 846 CASR
  • MGI:6194238
  • PMID:18852253
DOID:12466 secondary hyperparathyroidism HGNC:1514 Homo sapiens (human) 846 CASR
  • PMID:11044218
  • PMID:19640368
DOID:5844 myocardial infarction HGNC:1514 Homo sapiens (human) 846 CASR
  • MGI:6194238
DOID:13543 hyperparathyroidism HGNC:1514 Homo sapiens (human) 846 CASR
  • MGI:6194238
  • RGD:7240710
DOID:12678 hypercalcemia HGNC:1514 Homo sapiens (human) 846 CASR
  • PMID:20602573
DOID:0050700 cardiomyopathy HGNC:1514 Homo sapiens (human) 846 CASR
  • MGI:6194238
DOID:0111322 idiopathic generalized epilepsy 8 HGNC:1514 Homo sapiens (human) 846 CASR
  • RGD:7240710
DOID:0090107 autosomal dominant hypocalcemia 1 HGNC:1514 Homo sapiens (human) 846 CASR
  • MGI:6194238
  • RGD:7240710
DOID:0060700 familial hypocalciuric hypercalcemia 1 HGNC:1514 Homo sapiens (human) 846 CASR
  • MGI:6194238
  • PMID:21034470
  • PMID:7726161
  • PMID:7916660
  • RGD:7240710
DOID:6432 pulmonary hypertension HGNC:1514 Homo sapiens (human) 846 CASR
  • 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