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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 8001 - 8025 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:0081363
  • distal myopathy with rimmed vacuoles
Homo sapiens (human)
DOID:0110663
  • congenital myasthenic syndrome 1A
  • Aliases:
    • CMS IIa
    • CMS1A
    • congenital myasthenic syndrome 1A, slow-channel
    • congenital myasthenic syndrome type IIa
Mus musculus (house mouse)
DOID:12361
  • Graves' disease
  • Aliases:
    • Grave's disease
    • Graves disease
    • exophthalmic goiter
Saccharomyces cerevisiae S288C
DOID:13207
  • proliferative diabetic retinopathy
  • Aliases:
    • PDR
Saccharomyces cerevisiae S288C
DOID:936
  • brain disease
  • Aliases:
    • encephalopathy
Rattus norvegicus (Norway rat)
DOID:0060675
  • catecholaminergic polymorphic ventricular tachycardia 1
  • Aliases:
    • CVPT1
    • arrhythmogenic right ventricular dysplasia 2
Rattus norvegicus (Norway rat)
DOID:0111079
  • birdshot chorioretinopathy
  • Aliases:
    • BSCR
    • birdshot chorioretinitis
    • birdshot retinochoroiditis
    • birdshot retinochoroidopathy
    • vitiliginous choroiditis
Homo sapiens (human)
DOID:0080979
  • arthrogryposis multiplex congenita-3
Mus musculus (house mouse)
DOID:0111453
  • 2-aminoadipic 2-oxoadipic aciduria
  • Aliases:
    • AMOXAD
    • alpha-aminoadipic aciduria
Rattus norvegicus (Norway rat)
DOID:0050790
  • fibular hypoplasia and complex brachydactyly
  • Aliases:
    • Du Pan syndrome
    • acromesomelic dysplasia-2B
Homo sapiens (human)
DOID:0070256
  • congenital disorder of glycosylation type IId
  • Aliases:
    • CDG IId
    • CDG2D
    • CDGIId
Mus musculus (house mouse)
DOID:0111066
  • congenital bile acid synthesis defect 5
  • Aliases:
    • CBAS5
Saccharomyces cerevisiae S288C
DOID:0081046
  • frontonasal dysplasia 2
Homo sapiens (human)
DOID:0111727
  • geleophysic dysplasia 3
  • Aliases:
    • GPHYSD3
Mus musculus (house mouse)
DOID:0070433
  • hyperphosphatasia with impaired intellectual development syndrome 1
  • Aliases:
    • GPIBD2
    • HPMRS1
    • glycosylphosphatidylinositol biosynthesis defect 2
    • hyperphosphatasia with mental retardation syndrome 1
Xenopus tropicalis (tropical clawed frog)
DOID:0060060
  • non-Hodgkin lymphoma
Mus musculus (house mouse)
DOID:0050989
  • episodic ataxia type 1
Mus musculus (house mouse)
DOID:0060747
  • Duane-radial ray syndrome
  • Aliases:
    • DR syndrome
    • Duane anomaly with radial ray abnormalities and deafness
    • Okihiro syndrome
    • acrorenocular syndrome
Homo sapiens (human)
DOID:8719
  • in situ carcinoma
Saccharomyces cerevisiae S288C
DOID:0111681
  • glutamate-cysteine ligase deficiency
  • Aliases:
    • gamma-glutamylcysteine synthetase deficiency
    • hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency
Homo sapiens (human)
DOID:10230
  • aortic atherosclerosis
  • Aliases:
    • Atherosclerosis of aorta
Rattus norvegicus (Norway rat)
DOID:7736
  • retinal telangiectasia
Mus musculus (house mouse)
DOID:0050644
  • arterial calcification of infancy
  • Aliases:
    • generalized arterial calcification of infancy
    • idiopathic infantile arterial calcification
    • infantile arteriosclerosis
Mus musculus (house mouse)
DOID:2043
  • hepatitis B
  • Aliases:
    • chronic hepatitis B
    • hepatitis B infection
Saccharomyces cerevisiae S288C
DOID:0070442
  • paroxysmal nonkinesigenic dyskinesia 3
  • Aliases:
    • generalized epilepsy and paroxysmal dyskinesia
Mus musculus (house mouse)
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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