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 |
---|---|---|---|---|---|---|
Tay-Sachs disease, late-onset forms
|
HEXA
|
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Lysosomal Storage Diseases (LSDs)
|
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Gaucher disease, atypical, due to saposin C deficiency
|
PSAP
|
Lysosomal Storage Diseases (LSDs)
|
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Metachromatic leukodystrophy, due to saposin B deficiency
|
PSAP
|
|
Lysosomal Storage Diseases (LSDs)
|
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Combined saposin deficiency
|
PSAP
|
|
Lysosomal Storage Diseases (LSDs)
|
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Sandhoff disease
|
HEXB
|
|
Lysosomal Storage Diseases (LSDs)
|
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Sandhoff disease, infantile form
|
HEXB
|
Lysosomal Storage Diseases (LSDs)
|
||||
Sandhoff disease, juvenile form
|
HEXB
|
Lysosomal Storage Diseases (LSDs)
|
||||
Sandhoff disease, adult form
|
HEXB
|
Lysosomal Storage Diseases (LSDs)
|
||||
Mucopolysaccharidosis VII
|
GUSB
|
|
Lysosomal Storage Diseases (LSDs)
|
|||
Pompe disease
|
GAA
|
|
Lysosomal Storage Diseases (LSDs)
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01