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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 7476 - 7500 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source ▼
DOID:0112233
  • lissencephaly 8
  • Aliases:
    • LIS8
Xenopus laevis (African clawed frog)
DOID:0112233
  • lissencephaly 8
  • Aliases:
    • LIS8
Xenopus tropicalis (tropical clawed frog)
DOID:0112233
  • lissencephaly 8
  • Aliases:
    • LIS8
Rattus norvegicus (Norway rat)
DOID:0112233
  • lissencephaly 8
  • Aliases:
    • LIS8
Mus musculus (house mouse)
DOID:0112233
  • lissencephaly 8
  • Aliases:
    • LIS8
Danio rerio (zebrafish)
DOID:0112233
  • lissencephaly 8
  • Aliases:
    • LIS8
Homo sapiens (human)
DOID:0112232
  • lissencephaly 3
  • Aliases:
    • LIS3
Homo sapiens (human)
DOID:0112232
  • lissencephaly 3
  • Aliases:
    • LIS3
Mus musculus (house mouse)
DOID:0112231
  • lissencephaly 7 with cerebellar hypoplasia
  • Aliases:
    • LIS7
Rattus norvegicus (Norway rat)
DOID:0112231
  • lissencephaly 7 with cerebellar hypoplasia
  • Aliases:
    • LIS7
Homo sapiens (human)
DOID:0112230
  • lissencephaly 5
  • Aliases:
    • LIS5
Homo sapiens (human)
DOID:0112230
  • lissencephaly 5
  • Aliases:
    • LIS5
Caenorhabditis elegans
DOID:0112230
  • lissencephaly 5
  • Aliases:
    • LIS5
Mus musculus (house mouse)
DOID:0112228
  • lissencephaly 9 with complex brainstem malformation
  • Aliases:
    • LIS9
    • posterior-predominant lissencephaly-broad flat pons and medulla-midline crossing defects syndrome
Drosophila melanogaster (fruit fly)
DOID:0112228
  • lissencephaly 9 with complex brainstem malformation
  • Aliases:
    • LIS9
    • posterior-predominant lissencephaly-broad flat pons and medulla-midline crossing defects syndrome
Homo sapiens (human)
DOID:0112227
  • tubulinopathy
Homo sapiens (human)
DOID:0112227
  • tubulinopathy
Mus musculus (house mouse)
DOID:0112224
  • chondrodysplasia with joint dislocations gPAPP type
  • Aliases:
    • gPAPP deficiency
Mus musculus (house mouse)
DOID:0112224
  • chondrodysplasia with joint dislocations gPAPP type
  • Aliases:
    • gPAPP deficiency
Homo sapiens (human)
DOID:0112224
  • chondrodysplasia with joint dislocations gPAPP type
  • Aliases:
    • gPAPP deficiency
Rattus norvegicus (Norway rat)
DOID:0112223
  • developmental and epileptic encephalopathy 89
  • Aliases:
    • DEE89
    • early infantile epileptic encephalopathy 89
Homo sapiens (human)
DOID:0112223
  • developmental and epileptic encephalopathy 89
  • Aliases:
    • DEE89
    • early infantile epileptic encephalopathy 89
Mus musculus (house mouse)
DOID:0112222
  • developmental and epileptic encephalopathy 88
  • Aliases:
    • DEE88
    • early infantile epileptic encephalopathy 88
Mus musculus (house mouse)
DOID:0112222
  • developmental and epileptic encephalopathy 88
  • Aliases:
    • DEE88
    • early infantile epileptic encephalopathy 88
Homo sapiens (human)
DOID:0112221
  • developmental and epileptic encephalopathy 87
  • Aliases:
    • DEE87
    • early infantile epileptic encephalopathy 87
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