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 9926 - 9950 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▲ FlyGlycoDB Evidence References
DOID:13810 familial hypercholesterolemia HGNC:20001 Homo sapiens (human) 255738 PCSK9 inference by association of genotype from phenotype used in manual assertion
  • PMID:12730697
  • PMID:14727179
  • PMID:15772090
  • RGD:7240710
DOID:0112300 spondylometaphyseal dysplasia with cone-rod dystrophy HGNC:8754 Homo sapiens (human) 5130 PCYT1A inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050585 congenital generalized lipodystrophy HGNC:8754 Homo sapiens (human) 5130 PCYT1A inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0112343 hereditary spastic paraplegia 82 HGNC:8756 Homo sapiens (human) 5833 PCYT2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:2048 autoimmune hepatitis HGNC:8760 Homo sapiens (human) 5133 PDCD1 direct assay evidence used in manual assertion
  • PMID:23869988
DOID:9074 systemic lupus erythematosus HGNC:8760 Homo sapiens (human) 5133 PDCD1 inference by association of genotype from phenotype used in manual assertion
  • PMID:17228327
  • RGD:7240710
DOID:9074 systemic lupus erythematosus HGNC:8760 Homo sapiens (human) 5133 PDCD1 direct assay evidence used in manual assertion
  • PMID:19116915
DOID:0080162 lupus nephritis HGNC:8760 Homo sapiens (human) 5133 PDCD1 inference by association of genotype from phenotype used in manual assertion
  • PMID:15352422
  • PMID:15934088
DOID:2377 multiple sclerosis HGNC:8760 Homo sapiens (human) 5133 PDCD1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:684 hepatocellular carcinoma HGNC:8760 Homo sapiens (human) 5133 PDCD1 inference by association of genotype from phenotype used in manual assertion
  • PMID:27034168
DOID:2043 hepatitis B HGNC:8760 Homo sapiens (human) 5133 PDCD1 direct assay evidence used in manual assertion
  • PMID:31770816
DOID:2043 hepatitis B HGNC:8760 Homo sapiens (human) 5133 PDCD1 inference by association of genotype from phenotype used in manual assertion
  • PMID:28667037
  • PMID:29786123
DOID:1883 hepatitis C HGNC:8760 Homo sapiens (human) 5133 PDCD1 inference by association of genotype from phenotype used in manual assertion
  • PMID:25747035
DOID:0070296 primary autosomal recessive microcephaly HGNC:8766 Homo sapiens (human) 10015 PDCD6IP inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0060998 striatal degeneration 2 HGNC:8772 Homo sapiens (human) 10846 PDE10A inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0070547 primary pigmented nodular adrenocortical disease 2 HGNC:8773 Homo sapiens (human) 50940 PDE11A inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111247 hypertension and brachydactyly syndrome HGNC:8778 Homo sapiens (human) 5139 PDE3A inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050741 alcohol dependence HGNC:8781 Homo sapiens (human) 5142 PDE4B inference by association of genotype from phenotype used in manual assertion
  • PMID:18438686
DOID:2986 IgA glomerulonephritis HGNC:8784 Homo sapiens (human) 8654 PDE5A inference by association of genotype from phenotype used in manual assertion
  • PMID:20563733
DOID:0110375 retinitis pigmentosa 40 HGNC:8786 Homo sapiens (human) 5158 PDE6B inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110863 congenital stationary night blindness autosomal dominant 2 HGNC:8786 Homo sapiens (human) 5158 PDE6B inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3070 high grade glioma HGNC:8799 Homo sapiens (human) 5154 PDGFA mutant phenotype evidence used in manual assertion
  • PMID:21490965
DOID:11132 prostatic hypertrophy HGNC:8800 Homo sapiens (human) 5155 PDGFB mutant phenotype evidence used in manual assertion
  • PMID:22689130
DOID:0060230 basal ganglia calcification HGNC:8800 Homo sapiens (human) 5155 PDGFB inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:4467 clear cell renal cell carcinoma HGNC:8800 Homo sapiens (human) 5155 PDGFB direct assay evidence used in manual assertion
  • PMID:23879920
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