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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 11926 - 11950 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source ▲
DOID:2451
  • protein S deficiency
  • Aliases:
    • Protein S deficiency disease
Mus musculus (house mouse)
DOID:2451
  • protein S deficiency
  • Aliases:
    • Protein S deficiency disease
Homo sapiens (human)
DOID:2451
  • protein S deficiency
  • Aliases:
    • Protein S deficiency disease
Rattus norvegicus (Norway rat)
DOID:2452
  • thrombophilia
  • Aliases:
    • hypercoagulability state
Homo sapiens (human)
DOID:2452
  • thrombophilia
  • Aliases:
    • hypercoagulability state
Drosophila melanogaster (fruit fly)
DOID:2452
  • thrombophilia
  • Aliases:
    • hypercoagulability state
Mus musculus (house mouse)
DOID:2452
  • thrombophilia
  • Aliases:
    • hypercoagulability state
Caenorhabditis elegans
DOID:2452
  • thrombophilia
  • Aliases:
    • hypercoagulability state
Rattus norvegicus (Norway rat)
DOID:2468
  • psychotic disorder
  • Aliases:
    • mental or behavioural disorder
Mus musculus (house mouse)
DOID:2468
  • psychotic disorder
  • Aliases:
    • mental or behavioural disorder
Homo sapiens (human)
DOID:2468
  • psychotic disorder
  • Aliases:
    • mental or behavioural disorder
Drosophila melanogaster (fruit fly)
DOID:2475
  • chronic conjunctivitis
Homo sapiens (human)
DOID:2475
  • chronic conjunctivitis
Mus musculus (house mouse)
DOID:2475
  • chronic conjunctivitis
Rattus norvegicus (Norway rat)
DOID:2475
  • chronic conjunctivitis
Caenorhabditis elegans
DOID:2476
  • hereditary spastic paraplegia
  • Aliases:
    • French settlement disease
    • Strumpell-Lorrain disease
    • familial spastic paraplegia
    • hereditary spastic paraparesis
Danio rerio (zebrafish)
DOID:2476
  • hereditary spastic paraplegia
  • Aliases:
    • French settlement disease
    • Strumpell-Lorrain disease
    • familial spastic paraplegia
    • hereditary spastic paraparesis
Drosophila melanogaster (fruit fly)
DOID:2476
  • hereditary spastic paraplegia
  • Aliases:
    • French settlement disease
    • Strumpell-Lorrain disease
    • familial spastic paraplegia
    • hereditary spastic paraparesis
Saccharomyces cerevisiae S288C
DOID:2476
  • hereditary spastic paraplegia
  • Aliases:
    • French settlement disease
    • Strumpell-Lorrain disease
    • familial spastic paraplegia
    • hereditary spastic paraparesis
Homo sapiens (human)
DOID:2476
  • hereditary spastic paraplegia
  • Aliases:
    • French settlement disease
    • Strumpell-Lorrain disease
    • familial spastic paraplegia
    • hereditary spastic paraparesis
Xenopus tropicalis (tropical clawed frog)
DOID:2476
  • hereditary spastic paraplegia
  • Aliases:
    • French settlement disease
    • Strumpell-Lorrain disease
    • familial spastic paraplegia
    • hereditary spastic paraparesis
Rattus norvegicus (Norway rat)
DOID:2476
  • hereditary spastic paraplegia
  • Aliases:
    • French settlement disease
    • Strumpell-Lorrain disease
    • familial spastic paraplegia
    • hereditary spastic paraparesis
Mus musculus (house mouse)
DOID:2476
  • hereditary spastic paraplegia
  • Aliases:
    • French settlement disease
    • Strumpell-Lorrain disease
    • familial spastic paraplegia
    • hereditary spastic paraparesis
Caenorhabditis elegans
DOID:2477
  • motor peripheral neuropathy
  • Aliases:
    • HSMN
    • HSMN - Hereditary sensory and motor neuropathy
    • Hereditary motor and sensory neuropathy
    • Peripheral Motor Neuropathy
    • neuropathic muscular atrophy
Mus musculus (house mouse)
DOID:2477
  • motor peripheral neuropathy
  • Aliases:
    • HSMN
    • HSMN - Hereditary sensory and motor neuropathy
    • Hereditary motor and sensory neuropathy
    • Peripheral Motor Neuropathy
    • neuropathic muscular atrophy
Homo sapiens (human)
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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