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 13726 - 13750 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence References ▲
DOID:3969 papillary thyroid carcinoma HGNC:7102 Homo sapiens (human) 9562 MINPP1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0070137 autosomal recessive cutis laxa type IIB HGNC:9721 Homo sapiens (human) 5831 PYCR1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050676 Birt-Hogg-Dube syndrome HGNC:13995 Homo sapiens (human) 56980 PRDM10 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:11830 myopia HGNC:29222 Homo sapiens (human) 84146 ZNF644 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110061 amelogenesis imperfecta hypomaturation type 2A3 HGNC:26790 Homo sapiens (human) 256764 WDR72 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:5844 myocardial infarction HGNC:3467 Homo sapiens (human) 2099 ESR1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080596 hyper IgE recurrent infection syndrome 4 HGNC:6021 Homo sapiens (human) 3572 IL6ST inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0060162 dentatorubral-pallidoluysian atrophy HGNC:3033 Homo sapiens (human) 1822 ATN1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0070434 hyperphosphatasia with impaired intellectual development syndrome 2 HGNC:23215 Homo sapiens (human) 84720 PIGO inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111051 platelet-type bleeding disorder 18 HGNC:9879 Homo sapiens (human) 10235 RASGRP2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080591 Klippel-Feil syndrome 3 HGNC:4218 Homo sapiens (human) 9573 GDF3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0060174 GABA aminotransferase deficiency HGNC:23 Homo sapiens (human) 18 ABAT inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080716 infantile liver failure syndrome HGNC:15625 Homo sapiens (human) 51594 NBAS inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:8778 Crohn's disease HGNC:6018 Homo sapiens (human) 3569 IL6 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0070411 autosomal recessive spinocerebellar ataxia 30 HGNC:17663 Homo sapiens (human) 10531 PITRM1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0060438 Cole-Carpenter syndrome HGNC:8548 Homo sapiens (human) 5034 P4HB inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0070618 rhabdoid tumor predisposition syndrome 1 HGNC:11103 Homo sapiens (human) 6598 SMARCB1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080325 tuberous sclerosis 2 HGNC:5438 Homo sapiens (human) 3458 IFNG inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110612 primary ciliary dyskinesia 10 HGNC:20188 Homo sapiens (human) 55172 DNAAF2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:4644 epidermolysis bullosa simplex HGNC:1630 Homo sapiens (human) 977 CD151 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080633 developmental cardiac valvular defect HGNC:9067 Homo sapiens (human) 5337 PLD1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110660 congenital myasthenic syndrome 12 HGNC:4241 Homo sapiens (human) 2673 GFPT1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:891 progressive myoclonus epilepsy HGNC:10739 Homo sapiens (human) 10501 SEMA6B inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111581 C syndrome HGNC:16892 Homo sapiens (human) 10225 CD96 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:4479 pseudohypoaldosteronism HGNC:2553 Homo sapiens (human) 8452 CUL3 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
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