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 14076 - 14100 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence ▲ References
DOID:1790 malignant mesothelioma HGNC:172 Homo sapiens (human) 91 ACVR1B mutant phenotype evidence used in manual assertion
  • PMID:30061637
DOID:8761 acute megakaryocytic leukemia HGNC:6193 Homo sapiens (human) 3718 JAK3 mutant phenotype evidence used in manual assertion
  • PMID:16843266
DOID:9352 type 2 diabetes mellitus HGNC:4498 Homo sapiens (human) 2864 FFAR1 mutant phenotype evidence used in manual assertion
  • PMID:19401434
DOID:4914 esophagus adenocarcinoma HGNC:4567 Homo sapiens (human) 2886 GRB7 mutant phenotype evidence used in manual assertion
  • PMID:32737994
DOID:1240 leukemia HGNC:1014 Homo sapiens (human) 613 BCR mutant phenotype evidence used in manual assertion
  • PMID:11313935
DOID:693 dental enamel hypoplasia RGD:2332 Rattus norvegicus (Norway rat) 24255 Cftr mutant phenotype evidence used in manual assertion
  • PMID:31942562
DOID:0050855 renal fibrosis RGD:3870 Rattus norvegicus (Norway rat) 29260 Tlr4 mutant phenotype evidence used in manual assertion
  • PMID:22777483
DOID:1520 colon carcinoma HGNC:3766 Homo sapiens (human) 2323 FLT3LG mutant phenotype evidence used in manual assertion
  • PMID:10842197
DOID:5176 renal Wilms' tumor HGNC:1066 Homo sapiens (human) 648 BMI1 mutant phenotype evidence used in manual assertion
  • PMID:18467665
DOID:0050771 pheochromocytoma HGNC:4800 Homo sapiens (human) 3028 HSD17B10 mutant phenotype evidence used in manual assertion
  • PMID:25879199
DOID:687 hepatoblastoma HGNC:3002 Homo sapiens (human) 1800 DPEP1 mutant phenotype evidence used in manual assertion
  • PMID:31541079
DOID:409 liver disease HGNC:11784 Homo sapiens (human) 7056 THBD mutant phenotype evidence used in manual assertion
  • PMID:19487933
DOID:1793 pancreatic cancer HGNC:3148 Homo sapiens (human) 1890 TYMP mutant phenotype evidence used in manual assertion
  • PMID:19671868
DOID:10534 stomach cancer HGNC:28979 Homo sapiens (human) 23199 GSE1 mutant phenotype evidence used in manual assertion
  • PMID:29367342
DOID:7693 abdominal aortic aneurysm RGD:2493 Rattus norvegicus (Norway rat) 24310 Ace mutant phenotype evidence used in manual assertion
  • PMID:24602481
DOID:5199 ureteral obstruction RGD:2493 Rattus norvegicus (Norway rat) 24310 Ace mutant phenotype evidence used in manual assertion
  • PMID:21667191
DOID:0080199 colorectal carcinoma HGNC:1689 Homo sapiens (human) 966 CD59 mutant phenotype evidence used in manual assertion
  • PMID:12909127
DOID:3454 brain infarction RGD:620387 Rattus norvegicus (Norway rat) 83507 Parg mutant phenotype evidence used in manual assertion
  • PMID:12834903
DOID:6432 pulmonary hypertension HGNC:11050 Homo sapiens (human) 6532 SLC6A4 mutant phenotype evidence used in manual assertion
  • PMID:19736308
DOID:850 lung disease RGD:621320 Rattus norvegicus (Norway rat) 81687 Mmp9 mutant phenotype evidence used in manual assertion
  • PMID:19494493
  • PMID:19545667
DOID:332 amyotrophic lateral sclerosis HGNC:9237 Homo sapiens (human) 10891 PPARGC1A mutant phenotype evidence used in manual assertion
  • PMID:22102466
DOID:14791 Leber congenital amaurosis SGD:S000005772 Saccharomyces cerevisiae S288C 854420 ENV9 mutant phenotype evidence used in manual assertion
  • PMID:28540421
DOID:1793 pancreatic cancer HGNC:7637 Homo sapiens (human) 4673 NAP1L1 mutant phenotype evidence used in manual assertion
  • PMID:25071868
DOID:3070 high grade glioma HGNC:3416 Homo sapiens (human) 2057 EPOR mutant phenotype evidence used in manual assertion
  • PMID:21749867
DOID:10608 celiac disease HGNC:4944 Homo sapiens (human) 3119 HLA-DQB1 mutant phenotype evidence used in manual assertion
  • PMID:19494267
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