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 |
---|---|---|---|---|---|---|
Pompe disease, infantile-onset form
|
GAA
|
Lysosomal Storage Diseases (LSDs)
|
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Pompe disease, late-onset form
|
GAA
|
Lysosomal Storage Diseases (LSDs)
|
||||
Galactosialidosis
|
CTSA
|
|
Lysosomal Storage Diseases (LSDs)
|
|||
Duchenne muscular dystrophy
|
DMD
|
|
Congenital Disorders of Glycosylation (CDGs)
|
|||
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)
|
||||
B4GALT1-CDG
|
B4GALT1
|
|
Congenital Disorders of Glycosylation (CDGs)
|
|||
Sanfilippo syndrome D
|
GNS
|
|
Lysosomal Storage Diseases (LSDs)
|
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01