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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 6001 - 6025 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID ▲ Species Gene ID Gene Symbol FlyGlycoDB Evidence References
DOID:10003 sensorineural hearing loss HGNC:3535 Homo sapiens (human) 2147 F2 direct assay evidence used in manual assertion
  • PMID:18636032
DOID:3393 coronary artery disease HGNC:3535 Homo sapiens (human) 2147 F2 direct assay evidence used in manual assertion
  • PMID:14961168
DOID:10591 pre-eclampsia HGNC:3535 Homo sapiens (human) 2147 F2 inference by association of genotype from phenotype used in manual assertion
  • PMID:16246971
DOID:10608 celiac disease HGNC:3535 Homo sapiens (human) 2147 F2 direct assay evidence used in manual assertion
  • PMID:23556408
DOID:8337 appendicitis HGNC:3535 Homo sapiens (human) 2147 F2 direct assay evidence used in manual assertion
  • PMID:21663567
DOID:3526 cerebral infarction HGNC:3535 Homo sapiens (human) 2147 F2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0060903 thrombosis HGNC:3535 Homo sapiens (human) 2147 F2 inference by association of genotype from phenotype used in manual assertion
  • PMID:21070754
DOID:10003 sensorineural hearing loss HGNC:3535 Homo sapiens (human) 2147 F2 inference by association of genotype from phenotype used in manual assertion
  • PMID:17334320
DOID:3083 chronic obstructive pulmonary disease HGNC:3538 Homo sapiens (human) 2150 F2RL1 mutant phenotype evidence used in manual assertion
  • PMID:21245013
DOID:0060496 respiratory allergy HGNC:3538 Homo sapiens (human) 2150 F2RL1 direct assay evidence used in manual assertion
  • PMID:20186875
DOID:2841 asthma HGNC:3538 Homo sapiens (human) 2150 F2RL1 direct assay evidence used in manual assertion
  • PMID:19864598
DOID:12531 von Willebrand's disease HGNC:3541 Homo sapiens (human) 2152 F3 direct assay evidence used in manual assertion
  • PMID:4546024
DOID:0080600 COVID-19 HGNC:3541 Homo sapiens (human) 2152 F3 inference by association of genotype from phenotype used in manual assertion
  • PMID:32747830
DOID:0080630 B-lymphoblastic leukemia/lymphoma HGNC:3541 Homo sapiens (human) 2152 F3 direct assay evidence used in manual assertion
  • PMID:19874310
DOID:11247 disseminated intravascular coagulation HGNC:3541 Homo sapiens (human) 2152 F3 direct assay evidence used in manual assertion
  • PMID:3802033
DOID:5844 myocardial infarction HGNC:3542 Homo sapiens (human) 2153 F5 inference by association of genotype from phenotype used in manual assertion
  • PMID:15131548
DOID:2216 factor V deficiency HGNC:3542 Homo sapiens (human) 2153 F5 inference by association of genotype from phenotype used in manual assertion
  • PMID:11564077
  • RGD:7240710
DOID:0111902 thrombophilia due to activated protein C resistance HGNC:3542 Homo sapiens (human) 2153 F5 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0060903 thrombosis HGNC:3542 Homo sapiens (human) 2153 F5 inference by association of genotype from phenotype used in manual assertion
  • PMID:16549134
DOID:999 hypereosinophilic syndrome HGNC:3542 Homo sapiens (human) 2153 F5 inference by association of genotype from phenotype used in manual assertion
  • PMID:15026880
DOID:1612 breast cancer HGNC:3542 Homo sapiens (human) 2153 F5 inference by association of genotype from phenotype used in manual assertion
  • PMID:25407022
DOID:5082 liver cirrhosis HGNC:3542 Homo sapiens (human) 2153 F5 inference by association of genotype from phenotype used in manual assertion
  • PMID:26226452
DOID:783 end stage renal disease HGNC:3542 Homo sapiens (human) 2153 F5 inference by association of genotype from phenotype used in manual assertion
  • PMID:19520684
DOID:10003 sensorineural hearing loss HGNC:3542 Homo sapiens (human) 2153 F5 inference by association of genotype from phenotype used in manual assertion
  • PMID:16015153
DOID:11512 Budd-Chiari syndrome HGNC:3542 Homo sapiens (human) 2153 F5 inference by association of genotype from phenotype used in manual assertion
  • PMID:16825912
  • PMID:26238013
  • PMID:29771426
  • PMID:9245936
  • RGD:7240710
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International Collaboration

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: April 7, 2025