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 |
---|---|---|---|---|---|---|
Aspartylglucosaminuria
|
AGA
|
Lysosomal Storage Diseases (LSDs)
|
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Fucosidosis
|
FUCA1
|
Lysosomal Storage Diseases (LSDs)
|
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Alpha-mannosidosis
|
MAN2B1
|
|
Lysosomal Storage Diseases (LSDs)
|
|||
Alpha-mannosidosis, type I (early-onset)
|
MAN2B1
|
Lysosomal Storage Diseases (LSDs)
|
||||
Alpha-mannosidosis, type II (later-onset)
|
MAN2B1
|
Lysosomal Storage Diseases (LSDs)
|
||||
Beta-mannosidosis
|
MANBA
|
|
Lysosomal Storage Diseases (LSDs)
|
|||
Sialidosis
|
NEU1
|
|
Lysosomal Storage Diseases (LSDs)
|
|||
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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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01