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 101 - 125 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▼ Evidence References
DOID:2861 congenital nonspherocytic hemolytic anemia MGI:95797 Mus musculus (house mouse) 14751 Gpi1 author statement supported by traceable reference
  • PMID:8417789
DOID:0080600 COVID-19 HGNC:3541 Homo sapiens (human) 2152 F3 inference by association of genotype from phenotype used in manual assertion
  • PMID:32747830
DOID:1577 limited scleroderma HGNC:11365 Homo sapiens (human) 6775 STAT4 inference by association of genotype from phenotype used in manual assertion
  • PMID:19286670
  • PMID:23755762
DOID:8466 retinal degeneration HGNC:4893 Homo sapiens (human) 3082 HGF direct assay evidence used in manual assertion
  • PMID:15505072
DOID:0090075 hypogonadotropic hypogonadism 15 with or without anosmia HGNC:5201 Homo sapiens (human) 9394 HS6ST1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:874 bacterial pneumonia HGNC:6922 Homo sapiens (human) 4153 MBL2 inference by association of genotype from phenotype used in manual assertion
  • PMID:18641104
DOID:9352 type 2 diabetes mellitus HGNC:2595 Homo sapiens (human) 1543 CYP1A1 inference by association of genotype from phenotype used in manual assertion
  • PMID:11996959
DOID:0060868 leukoencephalopathy with vanishing white matter MGI:2446176 Mus musculus (house mouse) 224045 Eif2b5 author statement supported by traceable reference
  • PMID:20826436
  • PMID:23056417
  • PMID:26974157
  • PMID:30624206
DOID:0110875 holoprosencephaly 3 MGI:98297 Mus musculus (house mouse) 20423 Shh author statement supported by traceable reference
  • PMID:15105374
  • PMID:8837770
DOID:9263 homocystinuria HGNC:1550 Homo sapiens (human) 875 CBS inference by association of genotype from phenotype used in manual assertion
  • PMID:7506602
  • RGD:7240710
DOID:3969 papillary thyroid carcinoma HGNC:11825 Homo sapiens (human) 7080 NKX2-1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:1380 endometrial cancer HGNC:8905 Homo sapiens (human) 5236 PGM1 inference by association of genotype from phenotype used in manual assertion
  • PMID:508567
DOID:1094 attention deficit hyperactivity disorder HGNC:11050 Homo sapiens (human) 6532 SLC6A4 inference by association of genotype from phenotype used in manual assertion
  • PMID:27430630
DOID:0111278 histiocytosis-lymphadenopathy plus syndrome HGNC:23096 Homo sapiens (human) 55315 SLC29A3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3459 breast carcinoma HGNC:4948 Homo sapiens (human) 3123 HLA-DRB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:15382064
DOID:4483 rhinitis HGNC:5973 Homo sapiens (human) 3596 IL13 inference by association of genotype from phenotype used in manual assertion
  • PMID:20358028
  • PMID:20484924
DOID:10763 hypertension RGD:2703 Rattus norvegicus (Norway rat) 25051 Glp1r direct assay evidence used in manual assertion
  • PMID:12093887
DOID:0060041 autism spectrum disorder FB:FBgn0034136 Drosophila melanogaster (fruit fly) 36849 DAT combinatorial experimental and author inference evidence used in manual assertion
  • PMID:25774383
DOID:0050809 mucopolysaccharidosis IX HGNC:5320 Homo sapiens (human) 3373 HYAL1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:1168 familial hyperlipidemia HGNC:5233 Homo sapiens (human) 3304 HSPA1B inference by association of genotype from phenotype used in manual assertion
  • PMID:15992611
DOID:848 arthritis HGNC:4187 Homo sapiens (human) 2638 GC inference by association of genotype from phenotype used in manual assertion
  • PMID:21844150
DOID:9256 colorectal cancer HGNC:9673 Homo sapiens (human) 5795 PTPRJ inference by association of genotype from phenotype used in manual assertion
  • PMID:19672627
  • RGD:7240710
DOID:0111842 Keipert syndrome HGNC:4452 Homo sapiens (human) 2239 GPC4 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:1184 nephrotic syndrome MGI:1859637 Mus musculus (house mouse) 54631 Nphs1 author statement supported by traceable reference
  • PMID:11136707
  • PMID:12039968
  • PMID:12039988
DOID:4783 mesangial proliferative glomerulonephritis RGD:621880 Rattus norvegicus (Norway rat) 66018 Pdgfd mutant phenotype evidence used in manual assertion
  • PMID:17308324
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