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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 7976 - 8000 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source ▲
DOID:0111837
  • congenital nongoitrous hypothyroidism 8
  • Aliases:
    • CHNG8
Homo sapiens (human)
DOID:0111839
  • congenital disorder of glycosylation Icc
  • Aliases:
    • congenital disorder of glycosylation type Icc
Saccharomyces cerevisiae S288C
DOID:0111839
  • congenital disorder of glycosylation Icc
  • Aliases:
    • congenital disorder of glycosylation type Icc
Xenopus laevis (African clawed frog)
DOID:0111839
  • congenital disorder of glycosylation Icc
  • Aliases:
    • congenital disorder of glycosylation type Icc
Danio rerio (zebrafish)
DOID:0111839
  • congenital disorder of glycosylation Icc
  • Aliases:
    • congenital disorder of glycosylation type Icc
Rattus norvegicus (Norway rat)
DOID:0111839
  • congenital disorder of glycosylation Icc
  • Aliases:
    • congenital disorder of glycosylation type Icc
Drosophila melanogaster (fruit fly)
DOID:0111839
  • congenital disorder of glycosylation Icc
  • Aliases:
    • congenital disorder of glycosylation type Icc
Homo sapiens (human)
DOID:0111839
  • congenital disorder of glycosylation Icc
  • Aliases:
    • congenital disorder of glycosylation type Icc
Mus musculus (house mouse)
DOID:0111840
  • Van Esch-O'Driscoll syndrome
  • Aliases:
    • MRXSVEOD
    • VEODS
    • X-linked intellectual disability, Van Esch type
    • X-linked syndromic mental retardation Van Esch-O'Driscoll type
Saccharomyces cerevisiae S288C
DOID:0111840
  • Van Esch-O'Driscoll syndrome
  • Aliases:
    • MRXSVEOD
    • VEODS
    • X-linked intellectual disability, Van Esch type
    • X-linked syndromic mental retardation Van Esch-O'Driscoll type
Homo sapiens (human)
DOID:0111841
  • Shukla-Vernon syndrome
  • Aliases:
    • SHUVER
Homo sapiens (human)
DOID:0111841
  • Shukla-Vernon syndrome
  • Aliases:
    • SHUVER
Mus musculus (house mouse)
DOID:0111842
  • Keipert syndrome
  • Aliases:
    • KPTS
    • nasodigitoacoustic syndrome
Drosophila melanogaster (fruit fly)
DOID:0111842
  • Keipert syndrome
  • Aliases:
    • KPTS
    • nasodigitoacoustic syndrome
Homo sapiens (human)
DOID:0111842
  • Keipert syndrome
  • Aliases:
    • KPTS
    • nasodigitoacoustic syndrome
Mus musculus (house mouse)
DOID:0111843
  • Paganini-Miozzo syndrome
  • Aliases:
    • MRXSPM
Homo sapiens (human)
DOID:0111843
  • Paganini-Miozzo syndrome
  • Aliases:
    • MRXSPM
Danio rerio (zebrafish)
DOID:0111843
  • Paganini-Miozzo syndrome
  • Aliases:
    • MRXSPM
Xenopus tropicalis (tropical clawed frog)
DOID:0111843
  • Paganini-Miozzo syndrome
  • Aliases:
    • MRXSPM
Drosophila melanogaster (fruit fly)
DOID:0111843
  • Paganini-Miozzo syndrome
  • Aliases:
    • MRXSPM
Rattus norvegicus (Norway rat)
DOID:0111843
  • Paganini-Miozzo syndrome
  • Aliases:
    • MRXSPM
Mus musculus (house mouse)
DOID:0111844
  • X-linked intellectual developmental disorder 108
  • Aliases:
    • MRX108
Homo sapiens (human)
DOID:0111844
  • X-linked intellectual developmental disorder 108
  • Aliases:
    • MRX108
Saccharomyces cerevisiae S288C
DOID:0111844
  • X-linked intellectual developmental disorder 108
  • Aliases:
    • MRX108
Mus musculus (house mouse)
DOID:0111847
  • osteogenesis imperfecta type 19
  • Aliases:
    • OI19
    • osteogenesis imperfecta type XIX
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: August 19, 2024