GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB), DisGeNET, and Alliance of Genome Resources is integrated into one list.

Source Last Updated
Alliance of Genome Resources July 29, 2024
DisGeNET July 29, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 7326 - 7350 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source ▼
DOID:0080199
  • colorectal carcinoma
Rattus norvegicus (Norway rat)
DOID:0080178
  • mucositis
Mus musculus (house mouse)
DOID:0080178
  • mucositis
Rattus norvegicus (Norway rat)
DOID:0080176
  • meningococcal meningitis
Drosophila melanogaster (fruit fly)
DOID:0080176
  • meningococcal meningitis
Rattus norvegicus (Norway rat)
DOID:0080176
  • meningococcal meningitis
Mus musculus (house mouse)
DOID:0080162
  • lupus nephritis
Rattus norvegicus (Norway rat)
DOID:0080162
  • lupus nephritis
Mus musculus (house mouse)
DOID:0080158
  • herpes simplex virus keratitis
  • Aliases:
    • dendritic keratitis
Mus musculus (house mouse)
DOID:0080158
  • herpes simplex virus keratitis
  • Aliases:
    • dendritic keratitis
Drosophila melanogaster (fruit fly)
DOID:0080158
  • herpes simplex virus keratitis
  • Aliases:
    • dendritic keratitis
Rattus norvegicus (Norway rat)
DOID:0080153
  • medium chain acyl-CoA dehydrogenase deficiency
Mus musculus (house mouse)
DOID:0080153
  • medium chain acyl-CoA dehydrogenase deficiency
Rattus norvegicus (Norway rat)
DOID:0080139
  • multiple congenital anomalies-hypotonia-seizures syndrome 2
  • Aliases:
    • developmental and epileptic encephalopathy 20
    • early infantile epileptic encephalopathy 20
    • glycosylphosphatidylinositol biosynthesis defect 4
Rattus norvegicus (Norway rat)
DOID:0080139
  • multiple congenital anomalies-hypotonia-seizures syndrome 2
  • Aliases:
    • developmental and epileptic encephalopathy 20
    • early infantile epileptic encephalopathy 20
    • glycosylphosphatidylinositol biosynthesis defect 4
Xenopus laevis (African clawed frog)
DOID:0080139
  • multiple congenital anomalies-hypotonia-seizures syndrome 2
  • Aliases:
    • developmental and epileptic encephalopathy 20
    • early infantile epileptic encephalopathy 20
    • glycosylphosphatidylinositol biosynthesis defect 4
Caenorhabditis elegans
DOID:0080139
  • multiple congenital anomalies-hypotonia-seizures syndrome 2
  • Aliases:
    • developmental and epileptic encephalopathy 20
    • early infantile epileptic encephalopathy 20
    • glycosylphosphatidylinositol biosynthesis defect 4
Drosophila melanogaster (fruit fly)
DOID:0080139
  • multiple congenital anomalies-hypotonia-seizures syndrome 2
  • Aliases:
    • developmental and epileptic encephalopathy 20
    • early infantile epileptic encephalopathy 20
    • glycosylphosphatidylinositol biosynthesis defect 4
Mus musculus (house mouse)
DOID:0080139
  • multiple congenital anomalies-hypotonia-seizures syndrome 2
  • Aliases:
    • developmental and epileptic encephalopathy 20
    • early infantile epileptic encephalopathy 20
    • glycosylphosphatidylinositol biosynthesis defect 4
Danio rerio (zebrafish)
DOID:0080139
  • multiple congenital anomalies-hypotonia-seizures syndrome 2
  • Aliases:
    • developmental and epileptic encephalopathy 20
    • early infantile epileptic encephalopathy 20
    • glycosylphosphatidylinositol biosynthesis defect 4
Saccharomyces cerevisiae S288C
DOID:0080139
  • multiple congenital anomalies-hypotonia-seizures syndrome 2
  • Aliases:
    • developmental and epileptic encephalopathy 20
    • early infantile epileptic encephalopathy 20
    • glycosylphosphatidylinositol biosynthesis defect 4
Xenopus tropicalis (tropical clawed frog)
DOID:0080119
  • mitochondrial DNA depletion syndrome 1
  • Aliases:
    • mitochondrial DNA depletion syndrome 1 (MNGIE type)
    • mitochondrial neurogastrointestinal encephalopathy syndrome, TYMP-related
Rattus norvegicus (Norway rat)
DOID:0080119
  • mitochondrial DNA depletion syndrome 1
  • Aliases:
    • mitochondrial DNA depletion syndrome 1 (MNGIE type)
    • mitochondrial neurogastrointestinal encephalopathy syndrome, TYMP-related
Mus musculus (house mouse)
DOID:0080109
  • infantile myofibromatosis
  • Aliases:
    • lipofibromatosis
Drosophila melanogaster (fruit fly)
DOID:0080108
  • myoglobinuria
Saccharomyces cerevisiae S288C

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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