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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SLC35D1-CDG
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SLC35D1
|
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Congenital Disorders of Glycosylation (CDGs)
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Autosomal recessive multiple epiphyseal dysplasia
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SLC26A2
|
|
Congenital Disorders of Glycosylation (CDGs)
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Neonatal osseous dysplasia I
|
SLC26A2
|
|
Congenital Disorders of Glycosylation (CDGs)
|
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Achondrogenesis type IB
|
SLC26A2
|
|
Congenital Disorders of Glycosylation (CDGs)
|
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Diastrophic dysplasia
|
SLC26A2
|
|
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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Macular corneal dystrophy
|
CHST6
|
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Congenital Disorders of Glycosylation (CDGs)
|
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EXT1/EXT2-CDG
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EXT1,EXT2
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Congenital Disorders of Glycosylation (CDGs)
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B4GALT7-CDG
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B4GALT7
|
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Congenital Disorders of Glycosylation (CDGs)
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Nonaka myopathy
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GNE
|
|
Congenital Disorders of Glycosylation (CDGs)
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Partly supported by NIH Common Fund Grant #1U01GM125267-01