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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 201 - 225 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▼ Gene Symbol FlyGlycoDB Evidence References
DOID:0050884 triosephosphate isomerase deficiency SGD:S000002457 Saccharomyces cerevisiae S288C 851620 TPI1 genetic interaction evidence used in manual assertion
  • PMID:24598263
DOID:0050884 triosephosphate isomerase deficiency SGD:S000002457 Saccharomyces cerevisiae S288C 851620 TPI1 sequence similarity evidence used in manual assertion
  • PMID:24598263
DOID:162 cancer SGD:S000002457 Saccharomyces cerevisiae S288C 851620 TPI1 genetic interaction evidence used in manual assertion
  • PMID:26354769
DOID:162 cancer SGD:S000002457 Saccharomyces cerevisiae S288C 851620 TPI1 sequence similarity evidence used in manual assertion
  • PMID:26354769
DOID:3070 high grade glioma SGD:S000002224 Saccharomyces cerevisiae S288C 851493 IDP1 sequence similarity evidence used in manual assertion
  • PMID:27427385
DOID:3070 high grade glioma SGD:S000002224 Saccharomyces cerevisiae S288C 851493 IDP1 mutant phenotype evidence used in manual assertion
  • PMID:27427385
DOID:0060559 lethal congenital contracture syndrome 1 SGD:S000002366 Saccharomyces cerevisiae S288C 851320 GLE1 sequence similarity evidence used in manual assertion
  • PMID:24243016
DOID:0060559 lethal congenital contracture syndrome 1 SGD:S000002366 Saccharomyces cerevisiae S288C 851320 GLE1 genetic interaction evidence used in manual assertion
  • PMID:24243016
DOID:1289 neurodegenerative disease SGD:S000004295 Saccharomyces cerevisiae S288C 851013 ACO1 genetic interaction evidence used in manual assertion
  • PMID:25351951
DOID:331 central nervous system disease SGD:S000004295 Saccharomyces cerevisiae S288C 851013 ACO1 sequence similarity evidence used in manual assertion
  • PMID:25351951
DOID:1289 neurodegenerative disease SGD:S000004295 Saccharomyces cerevisiae S288C 851013 ACO1 sequence similarity evidence used in manual assertion
  • PMID:25351951
DOID:1891 optic nerve disease SGD:S000004295 Saccharomyces cerevisiae S288C 851013 ACO1 sequence similarity evidence used in manual assertion
  • PMID:25351951
DOID:0111442 optic atrophy 9 SGD:S000004295 Saccharomyces cerevisiae S288C 851013 ACO1 sequence similarity evidence used in manual assertion
  • PMID:33028849
DOID:331 central nervous system disease SGD:S000004295 Saccharomyces cerevisiae S288C 851013 ACO1 genetic interaction evidence used in manual assertion
  • PMID:25351951
DOID:0111442 optic atrophy 9 SGD:S000004295 Saccharomyces cerevisiae S288C 851013 ACO1 mutant phenotype evidence used in manual assertion
  • PMID:33028849
DOID:1891 optic nerve disease SGD:S000004295 Saccharomyces cerevisiae S288C 851013 ACO1 genetic interaction evidence used in manual assertion
  • PMID:25351951
DOID:0080417 developmental and epileptic encephalopathy 38 SGD:S000004232 Saccharomyces cerevisiae S288C 850943 ARV1 mutant phenotype evidence used in manual assertion
  • PMID:32449190
  • PMID:32462292
DOID:9455 lipid storage disease SGD:S000004232 Saccharomyces cerevisiae S288C 850943 ARV1 genetic interaction evidence used in manual assertion
  • PMID:24273168
DOID:0080417 developmental and epileptic encephalopathy 38 SGD:S000004232 Saccharomyces cerevisiae S288C 850943 ARV1 sequence similarity evidence used in manual assertion
  • PMID:27270415
  • PMID:32165008
  • PMID:32449190
  • PMID:32462292
DOID:0080417 developmental and epileptic encephalopathy 38 SGD:S000004232 Saccharomyces cerevisiae S288C 850943 ARV1 genetic interaction evidence used in manual assertion
  • PMID:27270415
DOID:9455 lipid storage disease SGD:S000004232 Saccharomyces cerevisiae S288C 850943 ARV1 sequence similarity evidence used in manual assertion
  • PMID:24273168
DOID:3070 high grade glioma SGD:S000004164 Saccharomyces cerevisiae S288C 850871 IDP2 mutant phenotype evidence used in manual assertion
  • PMID:27427385
DOID:3070 high grade glioma SGD:S000004164 Saccharomyces cerevisiae S288C 850871 IDP2 sequence similarity evidence used in manual assertion
  • PMID:27427385
DOID:0080552 congenital disorder of glycosylation Ia SGD:S000001849 Saccharomyces cerevisiae S288C 850499 SEC53 mutant phenotype evidence used in manual assertion
  • PMID:36214454
DOID:0080552 congenital disorder of glycosylation Ia SGD:S000001849 Saccharomyces cerevisiae S288C 850499 SEC53 genetic interaction evidence used in manual assertion
  • PMID:30530630
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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 8, 2025