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 |
---|---|---|---|---|---|---|
Gaucher disease, type III
|
GBA
|
|
Lysosomal Storage Diseases (LSDs)
|
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Gaucher disease, type IIIC
|
GBA
|
|
Lysosomal Storage Diseases (LSDs)
|
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Hereditary inclusion body myopathy type 2
|
GNE
|
|
Congenital Disorders of Glycosylation (CDGs)
|
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Hurler syndrome
|
IDUA
|
|
Lysosomal Storage Diseases (LSDs)
|
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Hurler-Scheie syndrome
|
IDUA
|
|
Lysosomal Storage Diseases (LSDs)
|
|||
Hyperphosphatasia with mental retardation syndrome 1
|
PIGV
|
|
Congenital Disorders of Glycosylation (CDGs)
|
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Krabbe disease
|
GALC
|
|
Lysosomal Storage Diseases (LSDs)
|
|||
Krabbe disease, infantile form
|
GALC
|
Lysosomal Storage Diseases (LSDs)
|
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Krabbe disease, late-onset form
|
GALC
|
Lysosomal Storage Diseases (LSDs)
|
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LARGE-CDG (cong. muscular dystrophy spectrum)
|
LARGE
|
|
Congenital Disorders of Glycosylation (CDGs)
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Partly supported by NIH Common Fund Grant #1U01GM125267-01