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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 3301 - 3325 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source ▲
DOID:0080065
  • autosomal recessive spinocerebellar ataxia 19
  • Aliases:
    • Lichtenstein-Knorr syndrome
    • SCAR19
Homo sapiens (human)
DOID:0080066
  • autosomal recessive spinocerebellar ataxia 20
  • Aliases:
    • SCAR20
Saccharomyces cerevisiae S288C
DOID:0080066
  • autosomal recessive spinocerebellar ataxia 20
  • Aliases:
    • SCAR20
Homo sapiens (human)
DOID:0080070
  • mucolipidosis II alpha/beta
  • Aliases:
    • I-cell disease
    • inclusion-cell disease
    • mucolipidosis II
Mus musculus (house mouse)
DOID:0080070
  • mucolipidosis II alpha/beta
  • Aliases:
    • I-cell disease
    • inclusion-cell disease
    • mucolipidosis II
Danio rerio (zebrafish)
DOID:0080071
  • mucolipidosis III alpha/beta
  • Aliases:
    • mucolipidosis III
    • pseudo-Hurler polydystrophy
Danio rerio (zebrafish)
DOID:0080071
  • mucolipidosis III alpha/beta
  • Aliases:
    • mucolipidosis III
    • pseudo-Hurler polydystrophy
Mus musculus (house mouse)
DOID:0080072
  • intestinal pseudo-obstruction
  • Aliases:
    • Chronic intestinal pseudo-obstruction
    • neuronal intestinal dysplasia
Saccharomyces cerevisiae S288C
DOID:0080072
  • intestinal pseudo-obstruction
  • Aliases:
    • Chronic intestinal pseudo-obstruction
    • neuronal intestinal dysplasia
Homo sapiens (human)
DOID:0080072
  • intestinal pseudo-obstruction
  • Aliases:
    • Chronic intestinal pseudo-obstruction
    • neuronal intestinal dysplasia
Mus musculus (house mouse)
DOID:0080074
  • neural tube defect
Homo sapiens (human)
DOID:0080074
  • neural tube defect
Mus musculus (house mouse)
DOID:0080075
  • Neu-Laxova syndrome 2
Homo sapiens (human)
DOID:0080076
  • Neu-Laxova syndrome 1
Homo sapiens (human)
DOID:0080077
  • hypophosphatemic nephrolithiasis/osteoporosis 1
Rattus norvegicus (Norway rat)
DOID:0080077
  • hypophosphatemic nephrolithiasis/osteoporosis 1
Mus musculus (house mouse)
DOID:0080077
  • hypophosphatemic nephrolithiasis/osteoporosis 1
Homo sapiens (human)
DOID:0080079
  • nonsyndromic congenital nail disorder 1
  • Aliases:
    • nonsyndromic congenital nail disorder 10
    • twenty-nail dystrophy
Caenorhabditis elegans
DOID:0080079
  • nonsyndromic congenital nail disorder 1
  • Aliases:
    • nonsyndromic congenital nail disorder 10
    • twenty-nail dystrophy
Mus musculus (house mouse)
DOID:0080079
  • nonsyndromic congenital nail disorder 1
  • Aliases:
    • nonsyndromic congenital nail disorder 10
    • twenty-nail dystrophy
Homo sapiens (human)
DOID:0080081
  • nonsyndromic congenital nail disorder 3
Xenopus laevis (African clawed frog)
DOID:0080081
  • nonsyndromic congenital nail disorder 3
Danio rerio (zebrafish)
DOID:0080081
  • nonsyndromic congenital nail disorder 3
Rattus norvegicus (Norway rat)
DOID:0080081
  • nonsyndromic congenital nail disorder 3
Mus musculus (house mouse)
DOID:0080081
  • nonsyndromic congenital nail disorder 3
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