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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
Mus musculus (house mouse)
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
Mus musculus (house mouse)
DOID:0110831
  • Usher syndrome type 1D
  • Aliases:
    • USH1D
    • Usher syndrome type ID
Drosophila melanogaster (fruit fly)
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
Rattus norvegicus (Norway rat)
DOID:0110832
  • Usher syndrome type 1F
  • Aliases:
    • USH1F
    • Usher syndrome type IF
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:0110838
  • Usher syndrome type 2A
  • Aliases:
    • USH2A
    • Usher syndrome type IIA
Homo sapiens (human)
DOID:0110838
  • Usher syndrome type 2A
  • Aliases:
    • USH2A
    • Usher syndrome type IIA
Mus musculus (house mouse)
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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

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Last updated: August 19, 2024