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 |
---|---|---|---|---|---|---|
Achondrogenesis type IB
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SLC26A2
|
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Congenital Disorders of Glycosylation (CDGs)
|
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ATP6VOA2-CDG
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ATP6V0A2
|
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Congenital Disorders of Glycosylation (CDGs)
|
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Farber Lipogranulomatosis
|
ASAH1
|
|
Lysosomal Storage Diseases (LSDs)
|
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Wolman disease
|
LIPA
|
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Lysosomal Storage Diseases (LSDs)
|
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Tay-Sachs disease, infantile form
|
HEXA
|
|
Lysosomal Storage Diseases (LSDs)
|
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Ehlers-Danlos syndrome, musculocontractural type
|
CHST14
|
|
Congenital Disorders of Glycosylation (CDGs)
|
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Fabry disease
|
GLA
|
|
Lysosomal Storage Diseases (LSDs)
|
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Alpha-mannosidosis
|
MAN2B1
|
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Lysosomal Storage Diseases (LSDs)
|
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ST3GAL5-CDG
|
SIAT9
|
|
Congenital Disorders of Glycosylation (CDGs)
|
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Neonatal osseous dysplasia I
|
SLC26A2
|
|
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