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 2626 - 2650 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence References
DOID:0070490 infantile parkinsonism-dystonia 2 HGNC:10935 Homo sapiens (human) 6571 SLC18A2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3312 bipolar disorder HGNC:10934 Homo sapiens (human) 6570 SLC18A1 inference by association of genotype from phenotype used in manual assertion
  • PMID:16936705
DOID:5419 schizophrenia HGNC:10934 Homo sapiens (human) 6570 SLC18A1 inference by association of genotype from phenotype used in manual assertion
  • PMID:18451639
DOID:0110555 autosomal dominant nonsyndromic deafness 25 HGNC:20151 Homo sapiens (human) 246213 SLC17A8 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3659 sialuria HGNC:10933 Homo sapiens (human) 26503 SLC17A5 inference by association of genotype from phenotype used in manual assertion
  • PMID:10581036
  • RGD:7240710
DOID:13189 gout HGNC:10931 Homo sapiens (human) 10786 SLC17A3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080453 developmental and epileptic encephalopathy 25 HGNC:23089 Homo sapiens (human) 284111 SLC13A5 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:10595 Charcot-Marie-Tooth disease HGNC:10914 Homo sapiens (human) 9990 SLC12A6 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0090003 agenesis of the corpus callosum with peripheral neuropathy HGNC:10914 Homo sapiens (human) 9990 SLC12A6 inference by association of genotype from phenotype used in manual assertion
  • PMID:16606917
  • RGD:7240710
DOID:0080460 developmental and epileptic encephalopathy 34 HGNC:13818 Homo sapiens (human) 57468 SLC12A5 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111315 obsolete idiopathic generalized epilepsy 14 HGNC:13818 Homo sapiens (human) 57468 SLC12A5 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050450 Gitelman syndrome HGNC:10912 Homo sapiens (human) 6559 SLC12A3 inference by association of genotype from phenotype used in manual assertion
  • PMID:16221718
  • RGD:7240710
DOID:10825 essential hypertension HGNC:10912 Homo sapiens (human) 6559 SLC12A3 inference by association of genotype from phenotype used in manual assertion
  • PMID:15480096
  • PMID:15824464
DOID:0112159 autosomal dominant nonsyndromic deafness 78 HGNC:10911 Homo sapiens (human) 6558 SLC12A2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:445 Bartter disease HGNC:10910 Homo sapiens (human) 6557 SLC12A1 inference by association of genotype from phenotype used in manual assertion
  • PMID:8640224
DOID:0110142 Bartter disease type 1 HGNC:10910 Homo sapiens (human) 6557 SLC12A1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:14330 Parkinson's disease HGNC:10908 Homo sapiens (human) 4891 SLC11A2 inference by association of genotype from phenotype used in manual assertion
  • PMID:21777657
DOID:332 amyotrophic lateral sclerosis HGNC:10908 Homo sapiens (human) 4891 SLC11A2 inference by association of genotype from phenotype used in manual assertion
  • PMID:21276595
DOID:11759 hypochromic anemia HGNC:10908 Homo sapiens (human) 4891 SLC11A2 inference by association of genotype from phenotype used in manual assertion
  • PMID:16439678
DOID:2355 anemia HGNC:10908 Homo sapiens (human) 4891 SLC11A2 inference by association of genotype from phenotype used in manual assertion
  • PMID:17510944
DOID:9744 type 1 diabetes mellitus HGNC:10907 Homo sapiens (human) 6556 SLC11A1 inference by association of genotype from phenotype used in manual assertion
  • PMID:15877293
  • PMID:19768110
  • PMID:21524304
DOID:8577 ulcerative colitis HGNC:10907 Homo sapiens (human) 6556 SLC11A1 inference by association of genotype from phenotype used in manual assertion
  • PMID:11929588
  • PMID:18340647
DOID:1024 leprosy HGNC:10907 Homo sapiens (human) 6556 SLC11A1 inference by association of genotype from phenotype used in manual assertion
  • PMID:10608779
  • PMID:15755200
DOID:2957 pulmonary tuberculosis HGNC:10907 Homo sapiens (human) 6556 SLC11A1 inference by association of genotype from phenotype used in manual assertion
  • PMID:21169917
  • PMID:24024195
DOID:13241 Behcet's disease HGNC:10907 Homo sapiens (human) 6556 SLC11A1 inference by association of genotype from phenotype used in manual assertion
  • PMID:18998137
Download data in CSV format Download data in TSV format Download data in JSON format
About Release Notes Help Feedback
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