GDGDB is a database of glycan-related diseases and their responsible genes.
Database | Last Updated |
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Glyco-Disease Genes Database (GDGDB) | January 25, 2017 |
Concept UI | Disease Name | Gene Symbol | Disease Name Aliases | Disease Type ▲ | UniProt ID | Disease IDs |
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Macular corneal dystrophy
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CHST6
|
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Congenital Disorders of Glycosylation (CDGs)
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Spondyloepimetaphyseal dysplasia, pakistani type
|
PAPSS2
|
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Congenital Disorders of Glycosylation (CDGs)
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Diastrophic dysplasia
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SLC26A2
|
|
Congenital Disorders of Glycosylation (CDGs)
|
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Achondrogenesis type IB
|
SLC26A2
|
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Congenital Disorders of Glycosylation (CDGs)
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Neonatal osseous dysplasia I
|
SLC26A2
|
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Congenital Disorders of Glycosylation (CDGs)
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Autosomal recessive multiple epiphyseal dysplasia
|
SLC26A2
|
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Congenital Disorders of Glycosylation (CDGs)
|
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SLC35D1-CDG
|
SLC35D1
|
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Congenital Disorders of Glycosylation (CDGs)
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Tn polyagglutination syndrome, somatic (SOMATIC MUTATION)
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C1GALT1C1
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Congenital Disorders of Glycosylation (CDGs)
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GALNT3-CDG
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GALNT3
|
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Congenital Disorders of Glycosylation (CDGs)
|
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B3GALTL-CDG
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B3GALTL
|
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Congenital Disorders of Glycosylation (CDGs)
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01