GDGDB is a database of glycan-related diseases and their responsible genes.
Database | Last Updated |
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Glyco-Disease Genes Database (GDGDB) | January 25, 2017 |
Concept UI ▲ | Disease Name | Gene Symbol | Disease Name Aliases | Disease Type | UniProt ID | Disease IDs |
---|---|---|---|---|---|---|
ATP6VOA2-CDG
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ATP6V0A2
|
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Congenital Disorders of Glycosylation (CDGs)
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SEC23B-CDG
|
SEC23B
|
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Congenital Disorders of Glycosylation (CDGs)
|
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POMT1/POMT2-CDG (cong. muscular dystrophy spectrum)
|
POMT1,POMT2
|
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Congenital Disorders of Glycosylation (CDGs)
|
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POMGNT1-CDG (cong. muscular dystrophy spectrum)
|
POMGNT1
|
|
Congenital Disorders of Glycosylation (CDGs)
|
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Fukuyama congenital muscular dystrophy
|
FKTN
|
|
Congenital Disorders of Glycosylation (CDGs)
|
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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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Muscular dystrophy, congenital, type 1C
|
FKRP
|
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Congenital Disorders of Glycosylation (CDGs)
|
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Muscular dystrophy, limb-girdle, type 2I
|
FKRP
|
|
Congenital Disorders of Glycosylation (CDGs)
|
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LARGE-CDG (cong. muscular dystrophy spectrum)
|
LARGE
|
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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