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
GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB) and Alliance of Genome Resources is integrated into one list.

Source Last Updated
Alliance of Genome Resources October 9, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 8076 - 8100 of 15957 in total
Disease ID Disease Name ▲ Gene Symbol Gene ID Organism Source
DOID:0111729
  • familial episodic pain syndrome 1
  • Aliases:
    • FEPS1
Rattus norvegicus (Norway rat)
DOID:0111730
  • familial episodic pain syndrome 2
  • Aliases:
    • FEPS2
Homo sapiens (human)
DOID:0111730
  • familial episodic pain syndrome 2
  • Aliases:
    • FEPS2
Rattus norvegicus (Norway rat)
DOID:0111730
  • familial episodic pain syndrome 2
  • Aliases:
    • FEPS2
Drosophila melanogaster (fruit fly)
DOID:0111730
  • familial episodic pain syndrome 2
  • Aliases:
    • FEPS2
Mus musculus (house mouse)
DOID:0111731
  • familial episodic pain syndrome 3
  • Aliases:
    • FEPS3
Mus musculus (house mouse)
DOID:0111731
  • familial episodic pain syndrome 3
  • Aliases:
    • FEPS3
Homo sapiens (human)
DOID:0111731
  • familial episodic pain syndrome 3
  • Aliases:
    • FEPS3
Drosophila melanogaster (fruit fly)
DOID:0111731
  • familial episodic pain syndrome 3
  • Aliases:
    • FEPS3
Rattus norvegicus (Norway rat)
DOID:0060652
  • familial erythrocytosis 1
  • Aliases:
    • ECYT1
    • autosomal dominant benign erythrocytosis
    • primary familial and congenital polycythemia
Homo sapiens (human)
DOID:0060652
  • familial erythrocytosis 1
  • Aliases:
    • ECYT1
    • autosomal dominant benign erythrocytosis
    • primary familial and congenital polycythemia
Mus musculus (house mouse)
DOID:0060652
  • familial erythrocytosis 1
  • Aliases:
    • ECYT1
    • autosomal dominant benign erythrocytosis
    • primary familial and congenital polycythemia
Xenopus laevis (African clawed frog)
DOID:0080338
  • familial erythrocytosis 3
  • Aliases:
    • ECYT3
Mus musculus (house mouse)
DOID:0080339
  • familial erythrocytosis 4
  • Aliases:
    • ECYT4
Homo sapiens (human)
DOID:0080290
  • familial erythrocytosis 5
  • Aliases:
    • ECYT5
Danio rerio (zebrafish)
DOID:0080290
  • familial erythrocytosis 5
  • Aliases:
    • ECYT5
Rattus norvegicus (Norway rat)
DOID:0080290
  • familial erythrocytosis 5
  • Aliases:
    • ECYT5
Homo sapiens (human)
DOID:0080290
  • familial erythrocytosis 5
  • Aliases:
    • ECYT5
Mus musculus (house mouse)
DOID:0111632
  • familial erythrocytosis 6
  • Aliases:
    • ECYT6
    • beta-globin type erythrocytosis
    • beta-globin type polycythemia
Homo sapiens (human)
DOID:0111631
  • familial erythrocytosis 7
  • Aliases:
    • ECYT7
    • alpha-globin type erythrocytosis
    • alpha-globin type polycythemia
Homo sapiens (human)
DOID:0111630
  • familial erythrocytosis 8
  • Aliases:
    • BPGM deficiency
    • DPGM deficiency
    • ECYT8
    • bisphosphoglycerate mutase deficiency
    • bisphosphoglyceromutase deficiency
    • diphosphoglycerate mutase deficiency of erythrocyte
    • hemolytic anemia due to diphosphoglycerate mutase deficiency
Homo sapiens (human)
DOID:0111630
  • familial erythrocytosis 8
  • Aliases:
    • BPGM deficiency
    • DPGM deficiency
    • ECYT8
    • bisphosphoglycerate mutase deficiency
    • bisphosphoglyceromutase deficiency
    • diphosphoglycerate mutase deficiency of erythrocyte
    • hemolytic anemia due to diphosphoglycerate mutase deficiency
Saccharomyces cerevisiae S288C
DOID:0111630
  • familial erythrocytosis 8
  • Aliases:
    • BPGM deficiency
    • DPGM deficiency
    • ECYT8
    • bisphosphoglycerate mutase deficiency
    • bisphosphoglyceromutase deficiency
    • diphosphoglycerate mutase deficiency of erythrocyte
    • hemolytic anemia due to diphosphoglycerate mutase deficiency
Mus musculus (house mouse)
DOID:0111542
  • familial expansile osteolysis
  • Aliases:
    • FEO
    • McCabe disease
    • hereditary expansile polyostotic osteolytic dysplasia
Homo sapiens (human)
DOID:0111542
  • familial expansile osteolysis
  • Aliases:
    • FEO
    • McCabe disease
    • hereditary expansile polyostotic osteolytic dysplasia
Mus musculus (house mouse)
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 v4.1.0

Last updated: December 9, 2024