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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 January 28, 2025
Displaying entries 10176 - 10200 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▲ FlyGlycoDB Evidence References
DOID:0090056 dystonia 12 HGNC:9039 Homo sapiens (human) 8398 PLA2G6 inference by association of genotype from phenotype used in manual assertion
  • PMID:19087156
DOID:2367 neuroaxonal dystrophy HGNC:9039 Homo sapiens (human) 8398 PLA2G6 inference by association of genotype from phenotype used in manual assertion
  • PMID:17033970
  • PMID:19138334
DOID:0060900 Parkinson's disease 14 HGNC:9039 Homo sapiens (human) 8398 PLA2G6 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:1936 atherosclerosis HGNC:9040 Homo sapiens (human) 7941 PLA2G7 inference by association of genotype from phenotype used in manual assertion
  • PMID:12590019
DOID:2841 asthma HGNC:9040 Homo sapiens (human) 7941 PLA2G7 inference by association of genotype from phenotype used in manual assertion
  • PMID:10733466
DOID:12554 hemolytic-uremic syndrome HGNC:9040 Homo sapiens (human) 7941 PLA2G7 inference by association of genotype from phenotype used in manual assertion
  • PMID:10873870
DOID:0080379 nephrotic syndrome type 2 HGNC:9040 Homo sapiens (human) 7941 PLA2G7 inference by association of genotype from phenotype used in manual assertion
  • PMID:9853251
DOID:3393 coronary artery disease HGNC:9040 Homo sapiens (human) 7941 PLA2G7 inference by association of genotype from phenotype used in manual assertion
  • PMID:15115767
DOID:2986 IgA glomerulonephritis HGNC:9040 Homo sapiens (human) 7941 PLA2G7 inference by association of genotype from phenotype used in manual assertion
  • PMID:12220450
DOID:9352 type 2 diabetes mellitus HGNC:9040 Homo sapiens (human) 7941 PLA2G7 direct assay evidence used in manual assertion
  • PMID:22399516
DOID:7693 abdominal aortic aneurysm HGNC:9040 Homo sapiens (human) 7941 PLA2G7 inference by association of genotype from phenotype used in manual assertion
  • PMID:11807372
DOID:0050851 glomerulosclerosis HGNC:9040 Homo sapiens (human) 7941 PLA2G7 mutant phenotype evidence used in manual assertion
  • PMID:16213192
DOID:576 proteinuria HGNC:9040 Homo sapiens (human) 7941 PLA2G7 inference by association of genotype from phenotype used in manual assertion
  • PMID:10430976
DOID:12134 factor VIII deficiency HGNC:9051 Homo sapiens (human) 5327 PLAT direct assay evidence used in manual assertion
  • PMID:1419807
DOID:0060573 von Willebrand's disease 1 HGNC:9051 Homo sapiens (human) 5327 PLAT direct assay evidence used in manual assertion
  • PMID:1419807
DOID:9352 type 2 diabetes mellitus HGNC:9051 Homo sapiens (human) 5327 PLAT direct assay evidence used in manual assertion
  • PMID:15901895
  • PMID:16724515
DOID:5844 myocardial infarction HGNC:9051 Homo sapiens (human) 5327 PLAT direct assay evidence used in manual assertion
  • PMID:7994806
DOID:2988 antiphospholipid syndrome HGNC:9051 Homo sapiens (human) 5327 PLAT direct assay evidence used in manual assertion
  • PMID:16320350
DOID:8283 peritonitis HGNC:9051 Homo sapiens (human) 5327 PLAT direct assay evidence used in manual assertion
  • PMID:18571586
DOID:10159 osteonecrosis HGNC:9051 Homo sapiens (human) 5327 PLAT inference by association of genotype from phenotype used in manual assertion
  • PMID:24025446
DOID:5844 myocardial infarction HGNC:9051 Homo sapiens (human) 5327 PLAT inference by association of genotype from phenotype used in manual assertion
  • PMID:11848437
DOID:11713 diabetic angiopathy HGNC:9051 Homo sapiens (human) 5327 PLAT direct assay evidence used in manual assertion
  • PMID:18945481
DOID:5844 myocardial infarction HGNC:9052 Homo sapiens (human) 5328 PLAU mutant phenotype evidence used in manual assertion
  • PMID:17653104
DOID:0111050 Quebec platelet disorder HGNC:9052 Homo sapiens (human) 5328 PLAU inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:8283 peritonitis HGNC:9052 Homo sapiens (human) 5328 PLAU direct assay evidence used in manual assertion
  • PMID:18571586
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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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: April 7, 2025