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 11551 - 11575 of 15957 in total
Disease ID ▼ Disease Name Gene Symbol Gene ID Organism Source
DOID:0080688
  • mosaic variegated aneuploidy syndrome
Homo sapiens (human)
DOID:0080687
  • reducing body myopathy 1B
Homo sapiens (human)
DOID:0080686
  • tubular aggregate myopathy 2
Danio rerio (zebrafish)
DOID:0080686
  • tubular aggregate myopathy 2
Rattus norvegicus (Norway rat)
DOID:0080686
  • tubular aggregate myopathy 2
Homo sapiens (human)
DOID:0080686
  • tubular aggregate myopathy 2
Mus musculus (house mouse)
DOID:0080685
  • aortic dissection
Xenopus laevis (African clawed frog)
DOID:0080685
  • aortic dissection
Rattus norvegicus (Norway rat)
DOID:0080685
  • aortic dissection
Homo sapiens (human)
DOID:0080685
  • aortic dissection
Caenorhabditis elegans
DOID:0080685
  • aortic dissection
Mus musculus (house mouse)
DOID:0080684
  • diffuse midline glioma, H3 K27M-mutant
  • Aliases:
    • diffuse intrinsic pontine glioma
Homo sapiens (human)
DOID:0080681
  • X-linked chronic idiopathic intestinal pseudo-obstruction
Homo sapiens (human)
DOID:0080679
  • neuronal intestinal dysplasia type A
Rattus norvegicus (Norway rat)
DOID:0080679
  • neuronal intestinal dysplasia type A
Drosophila melanogaster (fruit fly)
DOID:0080679
  • neuronal intestinal dysplasia type A
Homo sapiens (human)
DOID:0080679
  • neuronal intestinal dysplasia type A
Caenorhabditis elegans
DOID:0080679
  • neuronal intestinal dysplasia type A
Mus musculus (house mouse)
DOID:0080678
  • mucolipidosis III gamma
Mus musculus (house mouse)
DOID:0080678
  • mucolipidosis III gamma
Homo sapiens (human)
DOID:0080677
  • otospondylomegaepiphyseal dysplasia, autosomal dominant
Mus musculus (house mouse)
DOID:0080677
  • otospondylomegaepiphyseal dysplasia, autosomal dominant
Homo sapiens (human)
DOID:0080676
  • Stickler syndrome 1
Xenopus laevis (African clawed frog)
DOID:0080676
  • Stickler syndrome 1
Xenopus tropicalis (tropical clawed frog)
DOID:0080676
  • Stickler syndrome 1
Homo sapiens (human)

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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