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 ▼ |
---|---|---|---|---|---|---|
Farber Lipogranulomatosis, type 5
|
ASAH1
|
Lysosomal Storage Diseases (LSDs)
|
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Aspartylglucosaminuria
|
AGA
|
Lysosomal Storage Diseases (LSDs)
|
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Beta-mannosidosis
|
MANBA
|
|
Lysosomal Storage Diseases (LSDs)
|
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Sialidosis type I
|
NEU1
|
|
Lysosomal Storage Diseases (LSDs)
|
|||
Sialidosis type II
|
NEU1
|
|
Lysosomal Storage Diseases (LSDs)
|
|||
Sialidosis type II, congenital form
|
NEU1
|
Lysosomal Storage Diseases (LSDs)
|
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Sialidosis type II, infantile form
|
NEU1
|
Lysosomal Storage Diseases (LSDs)
|
||||
Sialidosis type II, juvenile form
|
NEU1
|
Lysosomal Storage Diseases (LSDs)
|
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Schindler disease, type I
|
NAGA
|
|
Lysosomal Storage Diseases (LSDs)
|
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Schindler disease, type II
|
NAGA
|
|
Lysosomal Storage Diseases (LSDs)
|
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01