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 |
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Mucolipidosis III (alpha/beta)
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GNPTAB
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Lysosomal Storage Diseases (LSDs)
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Metachromatic leukodystrophy, adult form
|
ARSA
|
Lysosomal Storage Diseases (LSDs)
|
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Tay-Sachs disease
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HEXA
|
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Lysosomal Storage Diseases (LSDs)
|
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Metachromatic leukodystrophy, due to saposin B deficiency
|
PSAP
|
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Lysosomal Storage Diseases (LSDs)
|
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SRD5A3-CDG
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SRD5A3
|
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Congenital Disorders of Glycosylation (CDGs)
|
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Pompe disease
|
GAA
|
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Lysosomal Storage Diseases (LSDs)
|
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Hurler syndrome
|
IDUA
|
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Lysosomal Storage Diseases (LSDs)
|
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POMT1/POMT2-CDG (cong. muscular dystrophy spectrum)
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POMT1,POMT2
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Congenital Disorders of Glycosylation (CDGs)
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ALG12-CDG
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ALG12
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Congenital Disorders of Glycosylation (CDGs)
|
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Wolman disease
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LIPA
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Lysosomal Storage Diseases (LSDs)
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01