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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 5826 - 5850 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID ▲ Species Gene ID Gene Symbol FlyGlycoDB Evidence References
DOID:0050545 visceral heterotaxy HGNC:33983 Homo sapiens (human) 653275 CFC1B inference by association of genotype from phenotype used in manual assertion
  • PMID:11062482
  • PMID:25423076
DOID:0111013 cone-rod dystrophy 3 HGNC:34 Homo sapiens (human) 24 ABCA4 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110354 retinitis pigmentosa 19 HGNC:34 Homo sapiens (human) 24 ABCA4 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110015 age related macular degeneration 2 HGNC:34 Homo sapiens (human) 24 ABCA4 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:8466 retinal degeneration HGNC:34 Homo sapiens (human) 24 ABCA4 inference by association of genotype from phenotype used in manual assertion
  • PMID:22661473
DOID:8501 fundus dystrophy HGNC:34 Homo sapiens (human) 24 ABCA4 inference by association of genotype from phenotype used in manual assertion
  • PMID:16546111
DOID:10584 retinitis pigmentosa HGNC:34 Homo sapiens (human) 24 ABCA4 inference by association of genotype from phenotype used in manual assertion
  • PMID:18024811
  • PMID:9466990
DOID:4448 macular degeneration HGNC:34 Homo sapiens (human) 24 ABCA4 inference by association of genotype from phenotype used in manual assertion
  • PMID:9295268
DOID:13810 familial hypercholesterolemia HGNC:3402 Homo sapiens (human) 2053 EPHX2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3393 coronary artery disease HGNC:3402 Homo sapiens (human) 2053 EPHX2 inference by association of genotype from phenotype used in manual assertion
  • PMID:14732757
DOID:10763 hypertension HGNC:3402 Homo sapiens (human) 2053 EPHX2 inference by association of genotype from phenotype used in manual assertion
  • PMID:20065888
DOID:0111670 primary hyperoxaluria type 1 HGNC:341 Homo sapiens (human) 189 AGXT inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:891 progressive myoclonus epilepsy HGNC:3413 Homo sapiens (human) 7957 EPM2A inference by association of genotype from phenotype used in manual assertion
  • PMID:9771710
DOID:1686 glaucoma HGNC:3415 Homo sapiens (human) 2056 EPO direct assay evidence used in manual assertion
  • PMID:17554621
DOID:13268 porphyria HGNC:3415 Homo sapiens (human) 2056 EPO direct assay evidence used in manual assertion
  • PMID:17435269
DOID:10652 Alzheimer's disease HGNC:3415 Homo sapiens (human) 2056 EPO direct assay evidence used in manual assertion
  • PMID:22004348
  • PMID:23813967
DOID:9743 diabetic neuropathy HGNC:3415 Homo sapiens (human) 2056 EPO mutant phenotype evidence used in manual assertion
  • PMID:19244253
DOID:224 transient cerebral ischemia HGNC:3415 Homo sapiens (human) 2056 EPO direct assay evidence used in manual assertion
  • PMID:24702327
DOID:6000 congestive heart failure HGNC:3415 Homo sapiens (human) 2056 EPO direct assay evidence used in manual assertion
  • PMID:20139114
DOID:3525 middle cerebral artery infarction HGNC:3415 Homo sapiens (human) 2056 EPO mutant phenotype evidence used in manual assertion
  • PMID:20547143
DOID:8947 diabetic retinopathy HGNC:3415 Homo sapiens (human) 2056 EPO inference by association of genotype from phenotype used in manual assertion
  • PMID:18458324
DOID:3021 acute kidney failure HGNC:3415 Homo sapiens (human) 2056 EPO direct assay evidence used in manual assertion
  • PMID:22209169
  • PMID:22235348
DOID:3070 high grade glioma HGNC:3415 Homo sapiens (human) 2056 EPO mutant phenotype evidence used in manual assertion
  • PMID:21749867
DOID:1289 neurodegenerative disease HGNC:3415 Homo sapiens (human) 2056 EPO direct assay evidence used in manual assertion
  • PMID:16339796
DOID:1184 nephrotic syndrome HGNC:3415 Homo sapiens (human) 2056 EPO direct assay evidence used in manual assertion
  • PMID:23128049
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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: April 7, 2025