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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 7201 - 7225 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:0110351
  • osteogenesis imperfecta type 11
  • Aliases:
    • OI11
    • osteogenesis imperfecta type XI
Mus musculus (house mouse)
DOID:0110703
  • hypotrichosis 6
  • Aliases:
    • Hypotrichosis, Localized, Autosomal Recessive 1
    • Hypt6
    • Lah1
    • Monilethrix-like hypotrichosis
    • autosomal recessive localized hypotrichosis
Homo sapiens (human)
DOID:0050731
  • vitamin B12 deficiency
  • Aliases:
    • cobalamin deficiency
    • hypocobalaminemia
Caenorhabditis elegans
DOID:0110895
  • inflammatory bowel disease 14
  • Aliases:
    • IBD14
Homo sapiens (human)
DOID:0080960
  • amelogenesis imperfecta type 2A6
  • Aliases:
    • Amelogenesis imperfecta, hypomaturation type, IIA6
Homo sapiens (human)
DOID:3390
  • palmoplantar keratosis
  • Aliases:
    • Keratosis palmaris et plantaris
    • Palmoplantar Keratoderma
    • palmo-plantar keratodermas
Homo sapiens (human)
DOID:0060496
  • respiratory allergy
  • Aliases:
    • airway allergy
Caenorhabditis elegans
DOID:0111053
  • platelet-type bleeding disorder 15
  • Aliases:
    • BDPLT15
    • autosomal dominant macrothrombocytopenia ACTN1-related
Homo sapiens (human)
DOID:0050589
  • inflammatory bowel disease
Xenopus laevis (African clawed frog)
DOID:11151
  • cholecystolithiasis
Caenorhabditis elegans
DOID:2739
  • Gilbert syndrome
  • Aliases:
    • Constitutional hyperbilirubinemia
    • Gilbert's disease
    • Gilbert's syndrome
    • Gilbert-Meulengracht syndrome
    • hereditary nonhemolytic jaundice
Saccharomyces cerevisiae S288C
DOID:13922
  • eosinophilic esophagitis
Rattus norvegicus (Norway rat)
DOID:0080845
  • omodysplasia 2
Xenopus laevis (African clawed frog)
DOID:11212
  • hydrophthalmos
Homo sapiens (human)
DOID:0080265
  • nephrotic syndrome type 14
Homo sapiens (human)
DOID:0080016
  • spina bifida
Drosophila melanogaster (fruit fly)
DOID:0081290
  • Antley-Bixler syndrome without disordered steroidogenesis
Danio rerio (zebrafish)
DOID:4467
  • clear cell renal cell carcinoma
  • Aliases:
    • Clear cell carcinoma of kidney
    • clear cell kidney carcinoma
    • conventional (Clear cell) renal cell carcinoma
    • conventional renal cell carcinoma
    • renal clear cell carcinoma
Drosophila melanogaster (fruit fly)
DOID:3324
  • mood disorder
  • Aliases:
    • episodic mood disorder
Mus musculus (house mouse)
DOID:0070143
  • autosomal recessive cutis laxa type III
  • Aliases:
    • De Barsy syndrome
    • cutis laxa-corneal clouding-intellectual disability syndrome
Homo sapiens (human)
DOID:8869
  • neuromyelitis optica
  • Aliases:
    • Devic's disease
    • Devic's syndrome
Caenorhabditis elegans
DOID:0111392
  • mucopolysaccharidosis type IVB
  • Aliases:
    • MPS IVB
    • MPS4B
    • Morquio disease type B
    • Morquio syndrome B
    • beta-D-galactosidase deficiency
    • mucopolysaccharidosis type IVB (Morquio)
Mus musculus (house mouse)
DOID:934
  • viral infectious disease
  • Aliases:
    • Viral Infection
    • Viral disease
    • virus infection
Rattus norvegicus (Norway rat)
DOID:0060263
  • porencephaly
Drosophila melanogaster (fruit fly)
DOID:0070093
  • schizophrenia 18
  • Aliases:
    • Chromosome 7q36.3 Duplication Syndrome, 362-Kb
    • SCZD18
Rattus norvegicus (Norway rat)
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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