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 |
---|---|---|---|---|---|---|
MGAT2-CDG
|
MGAT2
|
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Congenital Disorders of Glycosylation (CDGs)
|
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Beta-mannosidosis
|
MANBA
|
|
Lysosomal Storage Diseases (LSDs)
|
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Alpha-mannosidosis
|
MAN2B1
|
|
Lysosomal Storage Diseases (LSDs)
|
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Alpha-mannosidosis, type I (early-onset)
|
MAN2B1
|
Lysosomal Storage Diseases (LSDs)
|
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Alpha-mannosidosis, type II (later-onset)
|
MAN2B1
|
Lysosomal Storage Diseases (LSDs)
|
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Mental retardation, autosomal recessive 15
|
MAN1B1
|
|
Congenital Disorders of Glycosylation (CDGs)
|
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Wolman disease
|
LIPA
|
|
Lysosomal Storage Diseases (LSDs)
|
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LFNG-CDG
|
LFNG
|
|
Congenital Disorders of Glycosylation (CDGs)
|
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LARGE-CDG (cong. muscular dystrophy spectrum)
|
LARGE
|
|
Congenital Disorders of Glycosylation (CDGs)
|
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Hurler syndrome
|
IDUA
|
|
Lysosomal Storage Diseases (LSDs)
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01