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 6526 - 6550 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source ▲
DOID:0110818
  • hereditary spastic paraplegia 73
  • Aliases:
    • SPG73
    • autosomal dominant spastic paraplegia 73
    • autosomal dominant spastic paraplegia type 73
Homo sapiens (human)
DOID:0110819
  • hereditary spastic paraplegia 74
  • Aliases:
    • SPG74
    • autosomal recessive spastic paraplegia 74
Homo sapiens (human)
DOID:0110820
  • hereditary spastic paraplegia 75
  • Aliases:
    • SPG75
    • autosomal recessive spastic paraplegia 75
    • autosomal recessive spastic paraplegia type 75
Mus musculus (house mouse)
DOID:0110820
  • hereditary spastic paraplegia 75
  • Aliases:
    • SPG75
    • autosomal recessive spastic paraplegia 75
    • autosomal recessive spastic paraplegia type 75
Rattus norvegicus (Norway rat)
DOID:0110820
  • hereditary spastic paraplegia 75
  • Aliases:
    • SPG75
    • autosomal recessive spastic paraplegia 75
    • autosomal recessive spastic paraplegia type 75
Homo sapiens (human)
DOID:0110821
  • hereditary spastic paraplegia 76
  • Aliases:
    • SPG76
    • autosomal recessive spastic paraplegia 76
Homo sapiens (human)
DOID:0110823
  • hereditary spastic paraplegia 8
  • Aliases:
    • SPG8
    • autosomal dominant spastic paraplegia 8
    • autosomal dominant spastic paraplegia type 8
Homo sapiens (human)
DOID:0110824
  • hereditary spastic paraplegia 9A
  • Aliases:
    • AD-SPG9A
    • Cataracts motor neuropathy-short stature-skeletal anomalies syndrome
    • SPG9A
    • autosomal dominant complex spastic paraplegia type 9A
    • autosomal dominant spastic paraplegia 9A
    • cataracts with motor neuronopathy, short stature and skeletal abnormalities
    • spastic paraparesis with amyopathy, cataracts and gastroesophageal reflux
    • spastic paraparesis-amyopathy-cataracts-gastroesophageal reflux syndrome
Mus musculus (house mouse)
DOID:0110824
  • hereditary spastic paraplegia 9A
  • Aliases:
    • AD-SPG9A
    • Cataracts motor neuropathy-short stature-skeletal anomalies syndrome
    • SPG9A
    • autosomal dominant complex spastic paraplegia type 9A
    • autosomal dominant spastic paraplegia 9A
    • cataracts with motor neuronopathy, short stature and skeletal abnormalities
    • spastic paraparesis with amyopathy, cataracts and gastroesophageal reflux
    • spastic paraparesis-amyopathy-cataracts-gastroesophageal reflux syndrome
Homo sapiens (human)
DOID:0110825
  • hereditary spastic paraplegia 9B
  • Aliases:
    • SPG9B
    • autosomal recessive complex spastic paraplegia type 9B
    • autosomal recessive spastic paraplegia 9B
Mus musculus (house mouse)
DOID:0110825
  • hereditary spastic paraplegia 9B
  • Aliases:
    • SPG9B
    • autosomal recessive complex spastic paraplegia type 9B
    • autosomal recessive spastic paraplegia 9B
Homo sapiens (human)
DOID:0110826
  • Usher syndrome type 1
  • Aliases:
    • US1
    • USH1
Homo sapiens (human)
DOID:0110827
  • Usher syndrome type 2
  • Aliases:
    • USH2
Homo sapiens (human)
DOID:0110827
  • Usher syndrome type 2
  • Aliases:
    • USH2
Mus musculus (house mouse)
DOID:0110828
  • Usher syndrome type 3
  • Aliases:
    • USH3
Mus musculus (house mouse)
DOID:0110828
  • Usher syndrome type 3
  • Aliases:
    • USH3
Homo sapiens (human)
DOID:0110831
  • Usher syndrome type 1D
  • Aliases:
    • USH1D
    • Usher syndrome type ID
Homo sapiens (human)
DOID:0110831
  • Usher syndrome type 1D
  • Aliases:
    • USH1D
    • Usher syndrome type ID
Mus musculus (house mouse)
DOID:0110831
  • Usher syndrome type 1D
  • Aliases:
    • USH1D
    • Usher syndrome type ID
Rattus norvegicus (Norway rat)
DOID:0110831
  • Usher syndrome type 1D
  • Aliases:
    • USH1D
    • Usher syndrome type ID
Drosophila melanogaster (fruit fly)
DOID:0110832
  • Usher syndrome type 1F
  • Aliases:
    • USH1F
    • Usher syndrome type IF
Mus musculus (house mouse)
DOID:0110832
  • Usher syndrome type 1F
  • Aliases:
    • USH1F
    • Usher syndrome type IF
Homo sapiens (human)
DOID:0110832
  • Usher syndrome type 1F
  • Aliases:
    • USH1F
    • Usher syndrome type IF
Drosophila melanogaster (fruit fly)
DOID:0110838
  • Usher syndrome type 2A
  • Aliases:
    • USH2A
    • Usher syndrome type IIA
Mus musculus (house mouse)
DOID:0110838
  • Usher syndrome type 2A
  • Aliases:
    • USH2A
    • Usher syndrome type IIA
Homo sapiens (human)
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