Table Filtering
Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
LM-GlycoRepo
Repository for lectin-assisted multimodality data
Resources Genes Glycoproteins Lectins Glycolipids Glycans Pathways Diseases Organisms
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Other Information
Release Statistics Download
Tools
SugarDrawer GlycanBuilder Glycan Converters GlycoMaple GlycomeAtlas LM-GlycomeAtlas GALAXY MCAW GlycoSim GRable
Search Tools
Cross Search Glycan Search Publication Search Programmatic Access
Standards Ontologies Notations
Guidelines
MIRAGE
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 9851 - 9875 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▲ FlyGlycoDB Evidence References
DOID:0110567 autosomal dominant nonsyndromic deafness 41 MGI:2665170 Mus musculus (house mouse) 231602 P2rx2 author statement supported by traceable reference
  • PMID:33791800
DOID:1875 impotence RGD:3242 Rattus norvegicus (Norway rat) 25265 P2ry1 direct assay evidence used in manual assertion
  • PMID:19303093
DOID:0060903 thrombosis RGD:621681 Rattus norvegicus (Norway rat) 64803 P2ry12 mutant phenotype evidence used in manual assertion
  • PMID:19692114
DOID:7693 abdominal aortic aneurysm RGD:621681 Rattus norvegicus (Norway rat) 64803 P2ry12 mutant phenotype evidence used in manual assertion
  • PMID:19028049
DOID:0060692 platelet-type bleeding disorder 8 MGI:1918089 Mus musculus (house mouse) 70839 P2ry12 author statement supported by traceable reference
  • PMID:11413167
  • PMID:12897207
DOID:1875 impotence RGD:62088 Rattus norvegicus (Norway rat) 29597 P2ry2 direct assay evidence used in manual assertion
  • PMID:19303093
DOID:0110336 osteogenesis imperfecta type 8 HGNC:19316 Homo sapiens (human) 64175 P3H1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110336 osteogenesis imperfecta type 8 MGI:1888921 Mus musculus (house mouse) 56401 P3h1 author statement supported by traceable reference
  • PMID:20363744
DOID:11830 myopia HGNC:8547 Homo sapiens (human) 8974 P4HA2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0060438 Cole-Carpenter syndrome HGNC:8548 Homo sapiens (human) 5034 P4HB inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:11719 oculopharyngeal muscular dystrophy HGNC:8565 Homo sapiens (human) 8106 PABPN1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0070047 Schuurs-Hoeijmakers Syndrome HGNC:30032 Homo sapiens (human) 55690 PACS1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080446 developmental and epileptic encephalopathy 66 HGNC:23794 Homo sapiens (human) 23241 PACS2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050453 lissencephaly HGNC:8574 Homo sapiens (human) 5048 PAFAH1B1 inference by association of genotype from phenotype used in manual assertion
  • PMID:11115846
DOID:0112237 lissencephaly 1 HGNC:8574 Homo sapiens (human) 5048 PAFAH1B1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0060058 lymphoma HGNC:8575 Homo sapiens (human) 5049 PAFAH1B2 inference by association of genotype from phenotype used in manual assertion
  • PMID:11983068
DOID:1612 breast cancer HGNC:8590 Homo sapiens (human) 5058 PAK1 inference by association of genotype from phenotype used in manual assertion
  • PMID:17486065
DOID:5419 schizophrenia HGNC:8590 Homo sapiens (human) 5058 PAK1 direct assay evidence used in manual assertion
  • PMID:22458949
DOID:4450 renal cell carcinoma HGNC:8590 Homo sapiens (human) 5058 PAK1 mutant phenotype evidence used in manual assertion
  • PMID:17621631
DOID:0060074 ductal carcinoma in situ HGNC:8591 Homo sapiens (human) 5062 PAK2 direct assay evidence used in manual assertion
  • PMID:22886747
DOID:0112051 non-syndromic X-linked intellectual disability 30 HGNC:8592 Homo sapiens (human) 5063 PAK3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:1793 pancreatic cancer HGNC:26144 Homo sapiens (human) 79728 PALB2 inference by association of genotype from phenotype used in manual assertion
  • PMID:19264984
  • RGD:7240710
DOID:0050671 female breast cancer HGNC:26144 Homo sapiens (human) 79728 PALB2 inference by association of genotype from phenotype used in manual assertion
  • PMID:30303537
DOID:5683 hereditary breast ovarian cancer syndrome HGNC:26144 Homo sapiens (human) 79728 PALB2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111094 Fanconi anemia complementation group N HGNC:26144 Homo sapiens (human) 79728 PALB2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
Download data in CSV format Download data in TSV format Download data in JSON format
About Release Notes Help Feedback

Click here to visit the beta site.

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

Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International

GlyCosmos Portal v4.2.1

Last updated: April 7, 2025