GDGDB is a database of glycan-related diseases and their responsible genes.
Database | Last Updated |
---|---|
Glyco-Disease Genes Database (GDGDB) | January 25, 2017 |
Concept UI | Disease Name | Gene Symbol | Disease Name Aliases | Disease Type ▲ | UniProt ID | Disease IDs |
---|---|---|---|---|---|---|
Fabry disease
|
GLA
|
|
Lysosomal Storage Diseases (LSDs)
|
|||
Gaucher disease, type I
|
GBA
|
|
Lysosomal Storage Diseases (LSDs)
|
|||
Gaucher disease, type II
|
GBA
|
Lysosomal Storage Diseases (LSDs)
|
||||
Gaucher disease, type II, neuronopathic form, classic type
|
GBA
|
Lysosomal Storage Diseases (LSDs)
|
||||
Gaucher disease, type II, perinatal lethal form
|
GBA
|
Lysosomal Storage Diseases (LSDs)
|
||||
Gaucher disease, type III
|
GBA
|
|
Lysosomal Storage Diseases (LSDs)
|
|||
Gaucher disease, type IIIC
|
GBA
|
|
Lysosomal Storage Diseases (LSDs)
|
|||
Gaucher disease, atypical, due to saposin C deficiency
|
PSAP
|
Lysosomal Storage Diseases (LSDs)
|
||||
Krabbe disease
|
GALC
|
|
Lysosomal Storage Diseases (LSDs)
|
|||
Krabbe disease, infantile form
|
GALC
|
Lysosomal Storage Diseases (LSDs)
|
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Partly supported by NIH Common Fund Grant #1U01GM125267-01