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 |
---|---|---|---|---|---|---|
Muscular dystrophy, limb-girdle, type 2M
|
FKTN
|
|
Congenital Disorders of Glycosylation (CDGs)
|
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Cardiomyopathy, dilated, 1X
|
FKTN
|
|
Congenital Disorders of Glycosylation (CDGs)
|
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Fucosidosis
|
FUCA1
|
Lysosomal Storage Diseases (LSDs)
|
||||
Pompe disease
|
GAA
|
|
Lysosomal Storage Diseases (LSDs)
|
|||
Pompe disease, infantile-onset form
|
GAA
|
Lysosomal Storage Diseases (LSDs)
|
||||
Pompe disease, late-onset form
|
GAA
|
Lysosomal Storage Diseases (LSDs)
|
||||
Krabbe disease
|
GALC
|
|
Lysosomal Storage Diseases (LSDs)
|
|||
Krabbe disease, infantile form
|
GALC
|
Lysosomal Storage Diseases (LSDs)
|
||||
Krabbe disease, late-onset form
|
GALC
|
Lysosomal Storage Diseases (LSDs)
|
||||
Morquio syndrome A
|
GALNS
|
|
Lysosomal Storage Diseases (LSDs)
|
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01