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 ▲ |
---|---|---|---|---|---|---|
Metachromatic leukodystrophy, due to saposin B deficiency
|
PSAP
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Lysosomal Storage Diseases (LSDs)
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Niemann-Pick disease, type A
|
SMPD1
|
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Lysosomal Storage Diseases (LSDs)
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Niemann-Pick disease, type B
|
SMPD1
|
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Lysosomal Storage Diseases (LSDs)
|
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Niemann-Pick disease, type C1
|
NPC1
|
|
Lysosomal Storage Diseases (LSDs)
|
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Niemann-Pick disease, type C2
|
NPC2
|
Lysosomal Storage Diseases (LSDs)
|
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Combined saposin deficiency
|
PSAP
|
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Lysosomal Storage Diseases (LSDs)
|
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PMM2-CDG
|
PMM2
|
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Congenital Disorders of Glycosylation (CDGs)
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MPI-CDG
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MPI
|
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Congenital Disorders of Glycosylation (CDGs)
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ALG6-CDG
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ALG6
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Congenital Disorders of Glycosylation (CDGs)
|
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ALG3-CDG
|
ALG3
|
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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