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 |
---|---|---|---|---|---|---|
ALG6-CDG
|
ALG6
|
|
Congenital Disorders of Glycosylation (CDGs)
|
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ATP6VOA2-CDG
|
ATP6V0A2
|
|
Congenital Disorders of Glycosylation (CDGs)
|
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COG6-CDG
|
COG6
|
|
Congenital Disorders of Glycosylation (CDGs)
|
|||
Hereditary inclusion body myopathy type 2
|
GNE
|
|
Congenital Disorders of Glycosylation (CDGs)
|
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Nonaka myopathy
|
GNE
|
|
Congenital Disorders of Glycosylation (CDGs)
|
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DOLK-CDG
|
TMEM15
|
|
Congenital Disorders of Glycosylation (CDGs)
|
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COG5-CDG
|
COG5
|
|
Congenital Disorders of Glycosylation (CDGs)
|
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ST3GAL5-CDG
|
SIAT9
|
|
Congenital Disorders of Glycosylation (CDGs)
|
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Mental retardation, autosomal recessive 15
|
MAN1B1
|
|
Congenital Disorders of Glycosylation (CDGs)
|
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B4GALT7-CDG
|
B4GALT7
|
|
Congenital Disorders of Glycosylation (CDGs)
|
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01