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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 14901 - 14925 of 15957 in total
Disease ID Disease Name ▲ Gene Symbol Gene ID Organism Source
DOID:0050983
  • spinocerebellar ataxia type 36
Homo sapiens (human)
DOID:0050984
  • spinocerebellar ataxia type 37
Drosophila melanogaster (fruit fly)
DOID:0050984
  • spinocerebellar ataxia type 37
Homo sapiens (human)
DOID:0050985
  • spinocerebellar ataxia type 38
Homo sapiens (human)
DOID:0050985
  • spinocerebellar ataxia type 38
Saccharomyces cerevisiae S288C
DOID:0050957
  • spinocerebellar ataxia type 4
Homo sapiens (human)
DOID:0050986
  • spinocerebellar ataxia type 40
Homo sapiens (human)
DOID:0050882
  • spinocerebellar ataxia type 5
Homo sapiens (human)
DOID:0050882
  • spinocerebellar ataxia type 5
Mus musculus (house mouse)
DOID:0050956
  • spinocerebellar ataxia type 6
Mus musculus (house mouse)
DOID:0050956
  • spinocerebellar ataxia type 6
Drosophila melanogaster (fruit fly)
DOID:0050956
  • spinocerebellar ataxia type 6
Homo sapiens (human)
DOID:0050956
  • spinocerebellar ataxia type 6
Rattus norvegicus (Norway rat)
DOID:0050956
  • spinocerebellar ataxia type 6
Danio rerio (zebrafish)
DOID:0050958
  • spinocerebellar ataxia type 7
Homo sapiens (human)
DOID:0050958
  • spinocerebellar ataxia type 7
Mus musculus (house mouse)
DOID:0090115
  • spinocerebellar ataxia with axonal neuropathy 1
  • Aliases:
    • SCAN1
    • autosomal recessive spinocerebellar ataxia with axonal neuropathy 1
    • spinocerebellar ataxia with axonal neuropathy type 1
Homo sapiens (human)
DOID:0050755
  • spinocerebellar ataxia with axonal neuropathy 2
  • Aliases:
    • AOA2
    • SCAN2
    • SCAR1
    • ataxia with oculomotor apraxia type 2
    • autosomal recessive spinocerebellar ataxia 1
    • autosomal recessive spinocerebellar ataxia with axonal neuropathy 2
    • spinocerebellar ataxia with axonal neuropathy type 2
Mus musculus (house mouse)
DOID:0050755
  • spinocerebellar ataxia with axonal neuropathy 2
  • Aliases:
    • AOA2
    • SCAN2
    • SCAR1
    • ataxia with oculomotor apraxia type 2
    • autosomal recessive spinocerebellar ataxia 1
    • autosomal recessive spinocerebellar ataxia with axonal neuropathy 2
    • spinocerebellar ataxia with axonal neuropathy type 2
Homo sapiens (human)
DOID:0050750
  • splenic marginal zone lymphoma
Homo sapiens (human)
DOID:0050750
  • splenic marginal zone lymphoma
Mus musculus (house mouse)
DOID:0090026
  • split hand-foot malformation 6
  • Aliases:
    • SHFM6
Homo sapiens (human)
DOID:0090026
  • split hand-foot malformation 6
  • Aliases:
    • SHFM6
Mus musculus (house mouse)
DOID:0090026
  • split hand-foot malformation 6
  • Aliases:
    • SHFM6
Caenorhabditis elegans
DOID:0090026
  • split hand-foot malformation 6
  • Aliases:
    • SHFM6
Danio rerio (zebrafish)
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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: December 9, 2024