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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 14801 - 14825 of 15957 in total
Disease ID ▼ Disease Name Gene Symbol Gene ID Organism Source
DOID:0050957
  • spinocerebellar ataxia type 4
Homo sapiens (human)
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:0050955
  • spinocerebellar ataxia type 2
Mus musculus (house mouse)
DOID:0050955
  • spinocerebellar ataxia type 2
Homo sapiens (human)
DOID:0050955
  • spinocerebellar ataxia type 2
Drosophila melanogaster (fruit fly)
DOID:0050954
  • spinocerebellar ataxia type 1
Mus musculus (house mouse)
DOID:0050954
  • spinocerebellar ataxia type 1
Homo sapiens (human)
DOID:0050952
  • spastic ataxia
Mus musculus (house mouse)
DOID:0050951
  • hereditary ataxia
Rattus norvegicus (Norway rat)
DOID:0050951
  • hereditary ataxia
Mus musculus (house mouse)
DOID:0050951
  • hereditary ataxia
Drosophila melanogaster (fruit fly)
DOID:0050951
  • hereditary ataxia
Danio rerio (zebrafish)
DOID:0050951
  • hereditary ataxia
Saccharomyces cerevisiae S288C
DOID:0050951
  • hereditary ataxia
Homo sapiens (human)
DOID:0050950
  • autosomal recessive cerebellar ataxia
Homo sapiens (human)
DOID:0050949
  • autosomal recessive hypophosphatemic rickets
Mus musculus (house mouse)
DOID:0050949
  • autosomal recessive hypophosphatemic rickets
Homo sapiens (human)
DOID:0050948
  • autosomal dominant hypophosphatemic rickets
Rattus norvegicus (Norway rat)
DOID:0050948
  • autosomal dominant hypophosphatemic rickets
Mus musculus (house mouse)
DOID:0050948
  • autosomal dominant hypophosphatemic rickets
Homo sapiens (human)
DOID:0050947
  • hereditary hypophosphatemic rickets with hypercalciuria
Homo sapiens (human)
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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