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 |
---|---|---|---|---|---|---|
Mucopolysaccharidosis VII
|
GUSB
|
|
Lysosomal Storage Diseases (LSDs)
|
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Hurler-Scheie syndrome
|
IDUA
|
|
Lysosomal Storage Diseases (LSDs)
|
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Scheie syndrome
|
IDUA
|
|
Lysosomal Storage Diseases (LSDs)
|
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Mental retardation, autosomal recessive 12
|
ST3GAL3
|
|
Congenital Disorders of Glycosylation (CDGs)
|
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Mental retardation, autosomal recessive 15
|
MAN1B1
|
|
Congenital Disorders of Glycosylation (CDGs)
|
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Multiple sulfatase deficiency
|
SUMF1
|
|
Lysosomal Storage Diseases (LSDs)
|
|||
Macular corneal dystrophy
|
CHST6
|
|
Congenital Disorders of Glycosylation (CDGs)
|
|||
TUSC3-CDG
|
TUSC3
|
|
Congenital Disorders of Glycosylation (CDGs)
|
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Sialidosis
|
NEU1
|
|
Lysosomal Storage Diseases (LSDs)
|
|||
POMGNT1-CDG (cong. muscular dystrophy spectrum)
|
POMGNT1
|
|
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