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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 12626 - 12650 of 15957 in total
Disease ID ▼ Disease Name Gene Symbol Gene ID Organism Source
DOID:0080062
  • autosomal recessive spinocerebellar ataxia 13
  • Aliases:
    • SCAR13
Mus musculus (house mouse)
DOID:0080061
  • autosomal recessive spinocerebellar ataxia 2
  • Aliases:
    • SCAR2
Homo sapiens (human)
DOID:0080061
  • autosomal recessive spinocerebellar ataxia 2
  • Aliases:
    • SCAR2
Mus musculus (house mouse)
DOID:0080060
  • autosomal recessive spinocerebellar ataxia 12
  • Aliases:
    • SCAR12
Saccharomyces cerevisiae S288C
DOID:0080059
  • autosomal recessive spinocerebellar ataxia 7
  • Aliases:
    • SCAR7
Danio rerio (zebrafish)
DOID:0080059
  • autosomal recessive spinocerebellar ataxia 7
  • Aliases:
    • SCAR7
Mus musculus (house mouse)
DOID:0080059
  • autosomal recessive spinocerebellar ataxia 7
  • Aliases:
    • SCAR7
Rattus norvegicus (Norway rat)
DOID:0080059
  • autosomal recessive spinocerebellar ataxia 7
  • Aliases:
    • SCAR7
Homo sapiens (human)
DOID:0080058
  • autosomal recessive spinocerebellar ataxia 14
  • Aliases:
    • SCAR14
Homo sapiens (human)
DOID:0080056
  • achondrogenesis type II
Mus musculus (house mouse)
DOID:0080056
  • achondrogenesis type II
Xenopus tropicalis (tropical clawed frog)
DOID:0080056
  • achondrogenesis type II
Xenopus laevis (African clawed frog)
DOID:0080056
  • achondrogenesis type II
Homo sapiens (human)
DOID:0080056
  • achondrogenesis type II
Rattus norvegicus (Norway rat)
DOID:0080055
  • achondrogenesis type IB
  • Aliases:
    • achondrogenesis Fraccaro type
Rattus norvegicus (Norway rat)
DOID:0080055
  • achondrogenesis type IB
  • Aliases:
    • achondrogenesis Fraccaro type
Mus musculus (house mouse)
DOID:0080055
  • achondrogenesis type IB
  • Aliases:
    • achondrogenesis Fraccaro type
Homo sapiens (human)
DOID:0080054
  • achondrogenesis type IA
  • Aliases:
    • achondrogenesis Houston-Harris type
Homo sapiens (human)
DOID:0080053
  • Albright's hereditary osteodystrophy
  • Aliases:
    • Albright hereditary osteodystrophy
    • pseudohypoparathyroidism type 1a
Homo sapiens (human)
DOID:0080053
  • Albright's hereditary osteodystrophy
  • Aliases:
    • Albright hereditary osteodystrophy
    • pseudohypoparathyroidism type 1a
Mus musculus (house mouse)
DOID:0080052
  • acromesomelic dysplasia, Grebe type
  • Aliases:
    • acromesomelic dysplasia-2A
    • grebe chondrodysplasia
Mus musculus (house mouse)
DOID:0080052
  • acromesomelic dysplasia, Grebe type
  • Aliases:
    • acromesomelic dysplasia-2A
    • grebe chondrodysplasia
Homo sapiens (human)
DOID:0080051
  • acromesomelic dysplasia, Hunter-Thompson type
  • Aliases:
    • acromesomelic dwarfism
    • acromesomelic dysplasia-2C
Homo sapiens (human)
DOID:0080051
  • acromesomelic dysplasia, Hunter-Thompson type
  • Aliases:
    • acromesomelic dwarfism
    • acromesomelic dysplasia-2C
Mus musculus (house mouse)
DOID:0080050
  • acromesomelic dysplasia, Maroteaux type
  • Aliases:
    • acromesomelic dysplasia-1
Caenorhabditis elegans
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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