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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 6026 - 6050 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID ▲ Species Gene ID Gene Symbol FlyGlycoDB Evidence References
DOID:1727 retinal vein occlusion HGNC:3542 Homo sapiens (human) 2153 F5 inference by association of genotype from phenotype used in manual assertion
  • PMID:10511031
  • PMID:16113792
DOID:10159 osteonecrosis HGNC:3542 Homo sapiens (human) 2153 F5 inference by association of genotype from phenotype used in manual assertion
  • PMID:16968732
DOID:10591 pre-eclampsia HGNC:3542 Homo sapiens (human) 2153 F5 inference by association of genotype from phenotype used in manual assertion
  • PMID:16246971
DOID:6432 pulmonary hypertension HGNC:3542 Homo sapiens (human) 2153 F5 inference by association of genotype from phenotype used in manual assertion
  • PMID:20182352
DOID:3526 cerebral infarction HGNC:3542 Homo sapiens (human) 2153 F5 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9477 pulmonary embolism HGNC:3542 Homo sapiens (human) 2153 F5 inference by association of genotype from phenotype used in manual assertion
  • PMID:14996674
DOID:0050864 non-arteritic anterior ischemic optic neuropathy HGNC:3542 Homo sapiens (human) 2153 F5 inference by association of genotype from phenotype used in manual assertion
  • PMID:15043529
DOID:1588 thrombocytopenia HGNC:3544 Homo sapiens (human) 2155 F7 direct assay evidence used in manual assertion
  • PMID:19175492
DOID:10763 hypertension HGNC:3544 Homo sapiens (human) 2155 F7 direct assay evidence used in manual assertion
  • PMID:10450539
DOID:9970 obesity HGNC:3544 Homo sapiens (human) 2155 F7 direct assay evidence used in manual assertion
  • PMID:14513073
  • PMID:9258277
DOID:2215 factor VII deficiency HGNC:3544 Homo sapiens (human) 2155 F7 inference by association of genotype from phenotype used in manual assertion
  • PMID:1634227
  • PMID:26083983
  • RGD:7240710
DOID:9744 type 1 diabetes mellitus HGNC:3544 Homo sapiens (human) 2155 F7 direct assay evidence used in manual assertion
  • PMID:11146704
DOID:3526 cerebral infarction HGNC:3544 Homo sapiens (human) 2155 F7 direct assay evidence used in manual assertion
  • PMID:21998055
DOID:5844 myocardial infarction HGNC:3544 Homo sapiens (human) 2155 F7 inference by association of genotype from phenotype used in manual assertion
  • PMID:16116695
  • PMID:9420338
  • RGD:7240710
DOID:3393 coronary artery disease HGNC:3544 Homo sapiens (human) 2155 F7 inference by association of genotype from phenotype used in manual assertion
  • PMID:11334615
DOID:9256 colorectal cancer HGNC:3544 Homo sapiens (human) 2155 F7 mutant phenotype evidence used in manual assertion
  • PMID:19062044
DOID:9744 type 1 diabetes mellitus HGNC:3544 Homo sapiens (human) 2155 F7 inference by association of genotype from phenotype used in manual assertion
  • PMID:9686915
DOID:9352 type 2 diabetes mellitus HGNC:3544 Homo sapiens (human) 2155 F7 direct assay evidence used in manual assertion
  • PMID:10332679
  • PMID:11689270
DOID:2913 acute pancreatitis HGNC:3544 Homo sapiens (human) 2155 F7 direct assay evidence used in manual assertion
  • PMID:17506000
DOID:12134 factor VIII deficiency HGNC:3546 Homo sapiens (human) 2157 F8 inference by association of genotype from phenotype used in manual assertion
  • PMID:10612839
  • PMID:16786531
  • RGD:7240710
DOID:12134 factor VIII deficiency HGNC:3546 Homo sapiens (human) 2157 F8 mutant phenotype evidence used in manual assertion
  • PMID:10468616
DOID:0111899 X-linked thrombophilia due to factor IX defect HGNC:3551 Homo sapiens (human) 2158 F9 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:12259 hemophilia B HGNC:3551 Homo sapiens (human) 2158 F9 inference by association of genotype from phenotype used in manual assertion
  • PMID:2041805
  • PMID:2714791
  • PMID:2752145
  • RGD:7240710
DOID:12259 hemophilia B HGNC:3551 Homo sapiens (human) 2158 F9 direct assay evidence used in manual assertion
  • PMID:20351275
DOID:0080839 X-linked warfarin sensitivity HGNC:3551 Homo sapiens (human) 2158 F9 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
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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