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 |
---|---|---|---|---|---|---|
GM1-gangliosidosis, type I
|
GLB1
|
|
Lysosomal Storage Diseases (LSDs)
|
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GM1-gangliosidosis, type II
|
GLB1
|
|
Lysosomal Storage Diseases (LSDs)
|
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GM1-gangliosidosis, type III
|
GLB1
|
|
Lysosomal Storage Diseases (LSDs)
|
|||
GM2-gangliosidosis, AB variant
|
GM2A
|
|
Lysosomal Storage Diseases (LSDs)
|
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Galactosialidosis
|
CTSA
|
|
Lysosomal Storage Diseases (LSDs)
|
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Gaucher disease, atypical, due to saposin C deficiency
|
PSAP
|
Lysosomal Storage Diseases (LSDs)
|
||||
Gaucher disease, type I
|
GBA
|
|
Lysosomal Storage Diseases (LSDs)
|
|||
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)
|
||||
Gaucher disease, type II, perinatal lethal form
|
GBA
|
Lysosomal Storage Diseases (LSDs)
|
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Partly supported by NIH Common Fund Grant #1U01GM125267-01