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 13201 - 13225 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence ▲ References
DOID:5844 myocardial infarction HGNC:11179 Homo sapiens (human) 6647 SOD1 mutant phenotype evidence used in manual assertion
  • PMID:22006090
DOID:3587 pancreatic ductal carcinoma HGNC:11119 Homo sapiens (human) 6608 SMO mutant phenotype evidence used in manual assertion
  • PMID:16826192
DOID:7474 malignant pleural mesothelioma HGNC:1960 Homo sapiens (human) 1139 CHRNA7 mutant phenotype evidence used in manual assertion
  • PMID:18722110
DOID:3525 middle cerebral artery infarction RGD:621397 Rattus norvegicus (Norway rat) 84022 Ghsr mutant phenotype evidence used in manual assertion
  • PMID:19352052
DOID:5176 renal Wilms' tumor HGNC:17101 Homo sapiens (human) 23512 SUZ12 mutant phenotype evidence used in manual assertion
  • PMID:18467665
DOID:576 proteinuria RGD:69051 Rattus norvegicus (Norway rat) 59086 Tgfb1 mutant phenotype evidence used in manual assertion
  • PMID:23249995
DOID:10283 prostate cancer SGD:S000000966 Saccharomyces cerevisiae S288C 856911 CHD1 mutant phenotype evidence used in manual assertion
  • PMID:31222142
DOID:9120 amyloidosis HGNC:584 Homo sapiens (human) 325 APCS mutant phenotype evidence used in manual assertion
  • PMID:12015594
DOID:0070508 metabolic dysfunction and alcohol associated liver disease HGNC:404 Homo sapiens (human) 217 ALDH2 mutant phenotype evidence used in manual assertion
  • PMID:25457208
DOID:3770 pulmonary fibrosis HGNC:1952 Homo sapiens (human) 1131 CHRM3 mutant phenotype evidence used in manual assertion
  • PMID:18480105
DOID:3525 middle cerebral artery infarction HGNC:6000 Homo sapiens (human) 3557 IL1RN mutant phenotype evidence used in manual assertion
  • PMID:7790404
DOID:769 neuroblastoma HGNC:1910 Homo sapiens (human) 10036 CHAF1A mutant phenotype evidence used in manual assertion
  • PMID:24335960
DOID:9351 diabetes mellitus WB:WBGene00000898 Caenorhabditis elegans 175410 daf-2 mutant phenotype evidence used in manual assertion
  • PMID:35729173
DOID:850 lung disease RGD:2493 Rattus norvegicus (Norway rat) 24310 Ace mutant phenotype evidence used in manual assertion
  • PMID:19114890
DOID:6000 congestive heart failure RGD:3876 Rattus norvegicus (Norway rat) 24835 Tnf mutant phenotype evidence used in manual assertion
  • PMID:11668085
  • PMID:15210453
DOID:14330 Parkinson's disease RGD:3853 Rattus norvegicus (Norway rat) 25085 Th mutant phenotype evidence used in manual assertion
  • PMID:2573072
DOID:4492 avian influenza HGNC:9605 Homo sapiens (human) 5743 PTGS2 mutant phenotype evidence used in manual assertion
  • PMID:18613795
DOID:3910 lung adenocarcinoma HGNC:9585 Homo sapiens (human) 5727 PTCH1 mutant phenotype evidence used in manual assertion
  • PMID:33359005
DOID:12930 dilated cardiomyopathy HGNC:6993 Homo sapiens (human) 4205 MEF2A mutant phenotype evidence used in manual assertion
  • PMID:16469744
DOID:219 colon cancer HGNC:20815 Homo sapiens (human) 55818 KDM3A mutant phenotype evidence used in manual assertion
  • PMID:19858293
DOID:8924 autoimmune thrombocytopenic purpura HGNC:11935 Homo sapiens (human) 959 CD40LG mutant phenotype evidence used in manual assertion
  • PMID:18341638
DOID:10487 Hirschsprung's disease RGD:2536 Rattus norvegicus (Norway rat) 50672 Ednrb mutant phenotype evidence used in manual assertion
  • PMID:9739043
DOID:3070 high grade glioma HGNC:18039 Homo sapiens (human) 10765 KDM5B mutant phenotype evidence used in manual assertion
  • PMID:25450384
DOID:10763 hypertension RGD:2536 Rattus norvegicus (Norway rat) 50672 Ednrb mutant phenotype evidence used in manual assertion
  • PMID:10749572
DOID:3587 pancreatic ductal carcinoma HGNC:7508 Homo sapiens (human) 4582 MUC1 mutant phenotype evidence used in manual assertion
  • PMID:18713982
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 v4.4.0

Last updated: December 8, 2025