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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 3601 - 3625 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source ▲
DOID:0080264
  • exudative vitreoretinopathy 7
  • Aliases:
    • EVR7
Homo sapiens (human)
DOID:0080264
  • exudative vitreoretinopathy 7
  • Aliases:
    • EVR7
Rattus norvegicus (Norway rat)
DOID:0080265
  • nephrotic syndrome type 14
Saccharomyces cerevisiae S288C
DOID:0080265
  • nephrotic syndrome type 14
Homo sapiens (human)
DOID:0080266
  • primary ciliary dyskinesia 37
Homo sapiens (human)
DOID:0080267
  • autosomal dominant nonsyndromic deafness 71
Homo sapiens (human)
DOID:0080267
  • autosomal dominant nonsyndromic deafness 71
Mus musculus (house mouse)
DOID:0080268
  • autosomal dominant nonsyndromic deafness 72
Caenorhabditis elegans
DOID:0080268
  • autosomal dominant nonsyndromic deafness 72
Homo sapiens (human)
DOID:0080268
  • autosomal dominant nonsyndromic deafness 72
Rattus norvegicus (Norway rat)
DOID:0080268
  • autosomal dominant nonsyndromic deafness 72
Drosophila melanogaster (fruit fly)
DOID:0080268
  • autosomal dominant nonsyndromic deafness 72
Danio rerio (zebrafish)
DOID:0080268
  • autosomal dominant nonsyndromic deafness 72
Xenopus laevis (African clawed frog)
DOID:0080268
  • autosomal dominant nonsyndromic deafness 72
Mus musculus (house mouse)
DOID:0080269
  • autosomal dominant nonsyndromic deafness 73
Rattus norvegicus (Norway rat)
DOID:0080269
  • autosomal dominant nonsyndromic deafness 73
Mus musculus (house mouse)
DOID:0080269
  • autosomal dominant nonsyndromic deafness 73
Drosophila melanogaster (fruit fly)
DOID:0080272
  • nephrotic syndrome type 16
Rattus norvegicus (Norway rat)
DOID:0080272
  • nephrotic syndrome type 16
Homo sapiens (human)
DOID:0080272
  • nephrotic syndrome type 16
Mus musculus (house mouse)
DOID:0080280
  • gingival fibromatosis 5
Homo sapiens (human)
DOID:0080280
  • gingival fibromatosis 5
Mus musculus (house mouse)
DOID:0080281
  • schizophrenia 19
Mus musculus (house mouse)
DOID:0080281
  • schizophrenia 19
Homo sapiens (human)
DOID:0080282
  • developmental and epileptic encephalopathy 56
  • Aliases:
    • DEE56
    • early infantile epileptic encephalopathy 56
Mus musculus (house mouse)
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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