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 |
---|---|---|---|---|---|---|
SLC35A1-CDG
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SLC35A1
|
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Congenital Disorders of Glycosylation (CDGs)
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Diastrophic dysplasia
|
SLC26A2
|
|
Congenital Disorders of Glycosylation (CDGs)
|
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Achondrogenesis type IB
|
SLC26A2
|
|
Congenital Disorders of Glycosylation (CDGs)
|
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Neonatal osseous dysplasia I
|
SLC26A2
|
|
Congenital Disorders of Glycosylation (CDGs)
|
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Autosomal recessive multiple epiphyseal dysplasia
|
SLC26A2
|
|
Congenital Disorders of Glycosylation (CDGs)
|
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ST3GAL5-CDG
|
SIAT9
|
|
Congenital Disorders of Glycosylation (CDGs)
|
|||
Sanfilippo syndrome A
|
SGSH
|
|
Lysosomal Storage Diseases (LSDs)
|
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SEC23B-CDG
|
SEC23B
|
|
Congenital Disorders of Glycosylation (CDGs)
|
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RFT1-CDG
|
RFT1
|
|
Congenital Disorders of Glycosylation (CDGs)
|
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Gaucher disease, atypical, due to saposin C deficiency
|
PSAP
|
Lysosomal Storage Diseases (LSDs)
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Partly supported by NIH Common Fund Grant #1U01GM125267-01