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 826 - 850 of 15957 in total
Disease ID ▲ Disease Name Gene Symbol Gene ID Organism Source
DOID:0050791
  • persistent Mullerian duct syndrome
  • Aliases:
    • persistent Muellerian duct syndrome
Homo sapiens (human)
DOID:0050791
  • persistent Mullerian duct syndrome
  • Aliases:
    • persistent Muellerian duct syndrome
Rattus norvegicus (Norway rat)
DOID:0050791
  • persistent Mullerian duct syndrome
  • Aliases:
    • persistent Muellerian duct syndrome
Mus musculus (house mouse)
DOID:0050792
  • multiple cutaneous and mucosal venous malformations
  • Aliases:
    • VMCM
    • cutaneomucosal venous malformation
    • mucocutaneous venous malformations
Drosophila melanogaster (fruit fly)
DOID:0050792
  • multiple cutaneous and mucosal venous malformations
  • Aliases:
    • VMCM
    • cutaneomucosal venous malformation
    • mucocutaneous venous malformations
Homo sapiens (human)
DOID:0050792
  • multiple cutaneous and mucosal venous malformations
  • Aliases:
    • VMCM
    • cutaneomucosal venous malformation
    • mucocutaneous venous malformations
Mus musculus (house mouse)
DOID:0050792
  • multiple cutaneous and mucosal venous malformations
  • Aliases:
    • VMCM
    • cutaneomucosal venous malformation
    • mucocutaneous venous malformations
Danio rerio (zebrafish)
DOID:0050793
  • short QT syndrome
Rattus norvegicus (Norway rat)
DOID:0050793
  • short QT syndrome
Homo sapiens (human)
DOID:0050793
  • short QT syndrome
Mus musculus (house mouse)
DOID:0050793
  • short QT syndrome
Caenorhabditis elegans
DOID:0050794
  • multiple synostoses syndrome
Mus musculus (house mouse)
DOID:0050794
  • multiple synostoses syndrome
Rattus norvegicus (Norway rat)
DOID:0050794
  • multiple synostoses syndrome
Homo sapiens (human)
DOID:0050795
  • cone dystrophy
  • Aliases:
    • retinal cone dystrophy
Mus musculus (house mouse)
DOID:0050795
  • cone dystrophy
  • Aliases:
    • retinal cone dystrophy
Homo sapiens (human)
DOID:0050797
  • peroxisomal acyl-CoA oxidase deficiency
  • Aliases:
    • Peroxisomal acyl-coenzyme A oxidase
Homo sapiens (human)
DOID:0050797
  • peroxisomal acyl-CoA oxidase deficiency
  • Aliases:
    • Peroxisomal acyl-coenzyme A oxidase
Saccharomyces cerevisiae S288C
DOID:0050797
  • peroxisomal acyl-CoA oxidase deficiency
  • Aliases:
    • Peroxisomal acyl-coenzyme A oxidase
Drosophila melanogaster (fruit fly)
DOID:0050800
  • cerebral creatine deficiency syndrome 1
  • Aliases:
    • CEREBRAL CREATINE DEFICIENCY SYNDROME 1
    • SLC6A8 deficiency
    • creatine transporter deficiency
Mus musculus (house mouse)
DOID:0050800
  • cerebral creatine deficiency syndrome 1
  • Aliases:
    • CEREBRAL CREATINE DEFICIENCY SYNDROME 1
    • SLC6A8 deficiency
    • creatine transporter deficiency
Rattus norvegicus (Norway rat)
DOID:0050800
  • cerebral creatine deficiency syndrome 1
  • Aliases:
    • CEREBRAL CREATINE DEFICIENCY SYNDROME 1
    • SLC6A8 deficiency
    • creatine transporter deficiency
Homo sapiens (human)
DOID:0050802
  • Ehlers-Danlos syndrome spondylodysplastic type 2
  • Aliases:
    • EHLERS-DANLOS SYNDROME, PROGEROID TYPE, 2
    • Ehlers-Danlos syndrome progeroid type
Danio rerio (zebrafish)
DOID:0050802
  • Ehlers-Danlos syndrome spondylodysplastic type 2
  • Aliases:
    • EHLERS-DANLOS SYNDROME, PROGEROID TYPE, 2
    • Ehlers-Danlos syndrome progeroid type
Mus musculus (house mouse)
DOID:0050802
  • Ehlers-Danlos syndrome spondylodysplastic type 2
  • Aliases:
    • EHLERS-DANLOS SYNDROME, PROGEROID TYPE, 2
    • Ehlers-Danlos syndrome progeroid type
Drosophila melanogaster (fruit fly)

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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: December 9, 2024