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 |
---|---|---|---|---|---|---|
Maroteaux-Lamy syndrome, intermediate form
|
ARSB
|
Lysosomal Storage Diseases (LSDs)
|
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Mucopolysaccharidosis VII
|
GUSB
|
|
Lysosomal Storage Diseases (LSDs)
|
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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)
|
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Tay-Sachs disease
|
HEXA
|
|
Lysosomal Storage Diseases (LSDs)
|
|||
Tay-Sachs disease, infantile form
|
HEXA
|
|
Lysosomal Storage Diseases (LSDs)
|
|||
Tay-Sachs disease, late-onset forms
|
HEXA
|
|
Lysosomal Storage Diseases (LSDs)
|
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Sandhoff disease
|
HEXB
|
|
Lysosomal Storage Diseases (LSDs)
|
|||
Sandhoff disease, infantile form
|
HEXB
|
Lysosomal Storage Diseases (LSDs)
|
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01