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 |
---|---|---|---|---|---|---|
GALNT3-CDG
|
GALNT3
|
|
Congenital Disorders of Glycosylation (CDGs)
|
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Gaucher disease, type I
|
GBA
|
|
Lysosomal Storage Diseases (LSDs)
|
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Gaucher disease, type II
|
GBA
|
Lysosomal Storage Diseases (LSDs)
|
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Gaucher disease, type II, neuronopathic form, classic type
|
GBA
|
Lysosomal Storage Diseases (LSDs)
|
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Gaucher disease, type II, perinatal lethal form
|
GBA
|
Lysosomal Storage Diseases (LSDs)
|
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Gaucher disease, type III
|
GBA
|
|
Lysosomal Storage Diseases (LSDs)
|
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Gaucher disease, type IIIC
|
GBA
|
|
Lysosomal Storage Diseases (LSDs)
|
|||
GCS1-CDG
|
GCS1
|
|
Congenital Disorders of Glycosylation (CDGs)
|
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Myasthenia, congenital, with tubular aggregates 1
|
GFPT1
|
|
Congenital Disorders of Glycosylation (CDGs)
|
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Fabry disease
|
GLA
|
|
Lysosomal Storage Diseases (LSDs)
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01