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 13926 - 13950 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▲ Evidence References
DOID:9452 steatotic liver disease MGI:99457 Mus musculus (house mouse) 17202 Mc4r author statement supported by traceable reference
  • PMID:21906580
DOID:10608 celiac disease HGNC:4944 Homo sapiens (human) 3119 HLA-DQB1 mutant phenotype evidence used in manual assertion
  • PMID:19494267
DOID:0070155 hereditary sensory and autonomic neuropathy type 2A HGNC:14540 Homo sapiens (human) 65125 WNK1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:7148 rheumatoid arthritis HGNC:1602 Homo sapiens (human) 1230 CCR1 mutant phenotype evidence used in manual assertion
  • PMID:12860725
DOID:9538 multiple myeloma HGNC:2621 Homo sapiens (human) 1557 CYP2C19 inference by association of genotype from phenotype used in manual assertion
  • PMID:17666363
DOID:0050742 nicotine dependence HGNC:6528 Homo sapiens (human) 3936 LCP1 inference by association of genotype from phenotype used in manual assertion
  • PMID:18438686
DOID:4154 dentinogenesis imperfecta HGNC:3054 Homo sapiens (human) 1834 DSPP inference by association of genotype from phenotype used in manual assertion
  • PMID:11175790
  • RGD:7240710
DOID:9651 systolic heart failure HGNC:7940 Homo sapiens (human) 4879 NPPB direct assay evidence used in manual assertion
  • PMID:23122795
DOID:9256 colorectal cancer HGNC:27310 Homo sapiens (human) 201163 FLCN inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:2256 osteochondrodysplasia HGNC:2218 Homo sapiens (human) 1298 COL9A2 inference by association of genotype from phenotype used in manual assertion
  • PMID:8528240
DOID:0050989 episodic ataxia type 1 MGI:96654 Mus musculus (house mouse) 16485 Kcna1 author statement supported by traceable reference
  • PMID:12612586
DOID:552 pneumonia HGNC:2631 Homo sapiens (human) 1571 CYP2E1 inference by association of genotype from phenotype used in manual assertion
  • PMID:15928955
DOID:1380 endometrial cancer HGNC:2595 Homo sapiens (human) 1543 CYP1A1 inference by association of genotype from phenotype used in manual assertion
  • PMID:18318428
DOID:0060540 Hermansky-Pudlak syndrome 2 HGNC:566 Homo sapiens (human) 8546 AP3B1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3083 chronic obstructive pulmonary disease HGNC:10801 Homo sapiens (human) 6439 SFTPB inference by association of genotype from phenotype used in manual assertion
  • PMID:11589345
  • PMID:15315329
  • PMID:15817713
  • PMID:18550614
DOID:0060041 autism spectrum disorder RGD:620218 Rattus norvegicus (Norway rat) 81646 Creb1 direct assay evidence used in manual assertion
  • PMID:29218394
DOID:684 hepatocellular carcinoma HGNC:2505 Homo sapiens (human) 1493 CTLA4 inference by association of genotype from phenotype used in manual assertion
  • PMID:23432218
DOID:2841 asthma HGNC:1318 Homo sapiens (human) 718 C3 inference by association of genotype from phenotype used in manual assertion
  • PMID:15278436
  • PMID:16355111
  • PMID:18566738
  • PMID:20395963
DOID:4074 pancreatic adenocarcinoma HGNC:9801 Homo sapiens (human) 5879 RAC1 mutant phenotype evidence used in manual assertion
  • PMID:21037555
DOID:9074 systemic lupus erythematosus MGI:1346328 Mus musculus (house mouse) 23853 Def6 author statement supported by traceable reference
  • PMID:16470246
DOID:8029 sporadic breast cancer HGNC:3467 Homo sapiens (human) 2099 ESR1 direct assay evidence used in manual assertion
  • PMID:17932744
DOID:0112182 mismatch repair cancer syndrome HGNC:21686 Homo sapiens (human) 8635 RNASET2 inference by association of genotype from phenotype used in manual assertion
  • PMID:28218421
DOID:4990 essential tremor HGNC:3024 Homo sapiens (human) 1814 DRD3 inference by association of genotype from phenotype used in manual assertion
  • PMID:16650084
DOID:3083 chronic obstructive pulmonary disease HGNC:286 Homo sapiens (human) 154 ADRB2 inference by association of genotype from phenotype used in manual assertion
  • PMID:18667995
  • PMID:18789663
  • PMID:19747908
  • PMID:20525719
DOID:0050578 occult macular dystrophy HGNC:15946 Homo sapiens (human) 94137 RP1L1 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 v4.4.0

Last updated: December 8, 2025