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 |
---|---|---|---|---|---|---|
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)
|
||||
Gaucher disease, atypical, due to saposin C deficiency
|
PSAP
|
Lysosomal Storage Diseases (LSDs)
|
||||
Krabbe disease, infantile form
|
GALC
|
Lysosomal Storage Diseases (LSDs)
|
||||
Krabbe disease, late-onset form
|
GALC
|
Lysosomal Storage Diseases (LSDs)
|
||||
Metachromatic leukodystrophy
|
ARSA
|
Lysosomal Storage Diseases (LSDs)
|
||||
Metachromatic leukodystrophy, infantile form
|
ARSA
|
Lysosomal Storage Diseases (LSDs)
|
||||
Metachromatic leukodystrophy, juvenile form
|
ARSA
|
Lysosomal Storage Diseases (LSDs)
|
||||
Metachromatic leukodystrophy, adult form
|
ARSA
|
Lysosomal Storage Diseases (LSDs)
|
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Partly supported by NIH Common Fund Grant #1U01GM125267-01