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 |
---|---|---|---|---|---|---|
Mucopolysaccharidosis II
|
IDS
|
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Lysosomal Storage Diseases (LSDs)
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Mucopolysaccharidosis VI
|
ARSB
|
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Lysosomal Storage Diseases (LSDs)
|
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Mucopolysaccharidosis VII
|
GUSB
|
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Lysosomal Storage Diseases (LSDs)
|
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Multiple congenital anomalies-hypotonia-seizures syndrome 1
|
PIGN
|
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Congenital Disorders of Glycosylation (CDGs)
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Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects
|
B3GAT3
|
Congenital Disorders of Glycosylation (CDGs)
|
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Multiple sulfatase deficiency
|
SUMF1
|
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Lysosomal Storage Diseases (LSDs)
|
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Muscular dystrophy, congenital, type 1C
|
FKRP
|
|
Congenital Disorders of Glycosylation (CDGs)
|
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Muscular dystrophy, limb-girdle, type 2I
|
FKRP
|
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Congenital Disorders of Glycosylation (CDGs)
|
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Muscular dystrophy, limb-girdle, type 2M
|
FKTN
|
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Congenital Disorders of Glycosylation (CDGs)
|
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Myasthenia, congenital, with tubular aggregates 1
|
GFPT1
|
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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