GDGDB is a database of glycan-related diseases and their responsible genes.
Source | 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 |
---|---|---|---|---|---|---|
CON00005 | Aspartylglucosaminuria | AGA |
|
Lysosomal Storage Diseases (LSDs) | P20933 | |
CON00353 | ALG1-CDG | ALG1 |
|
Congenital Disorders of Glycosylation (CDGs) | Q9BT22 | |
CON00621 | ALG11-CDG | ALG11 |
|
Congenital Disorders of Glycosylation (CDGs) | Q2TAA5 | |
CON00349 | ALG12-CDG | ALG12 |
|
Congenital Disorders of Glycosylation (CDGs) | Q9BV10 | |
CON00624 | ALG13-CDG | ALG13 |
|
Congenital Disorders of Glycosylation (CDGs) | Q9NP73 | |
CON00351 | ALG2-CDG | ALG2 |
|
Congenital Disorders of Glycosylation (CDGs) | Q9H553 | |
CON00346 | ALG3-CDG | ALG3 |
|
Congenital Disorders of Glycosylation (CDGs) | Q92685 | |
CON00345 | ALG6-CDG | ALG6 |
|
Congenital Disorders of Glycosylation (CDGs) | Q9Y672 | |
CON00350 | ALG8-CDG | ALG8 |
|
Congenital Disorders of Glycosylation (CDGs) | Q9BVK2 | |
CON00354 | ALG9-CDG | ALG9 |
|
Congenital Disorders of Glycosylation (CDGs) | Q9H6U8 | |
CON00080 | Metachromatic leukodystrophy | ARSA |
|
Lysosomal Storage Diseases (LSDs) | P15289 | |
CON00081 | Metachromatic leukodystrophy, infantile form | ARSA |
|
Lysosomal Storage Diseases (LSDs) | P15289 | |
CON00082 | Metachromatic leukodystrophy, juvenile form | ARSA |
|
Lysosomal Storage Diseases (LSDs) | P15289 | |
CON00083 | Metachromatic leukodystrophy, adult form | ARSA |
|
Lysosomal Storage Diseases (LSDs) | P15289 | |
CON00041 | Mucopolysaccharidosis VI | ARSB |
|
Lysosomal Storage Diseases (LSDs) | P15848 | |
CON00042 | Maroteaux-Lamy syndrome, severe form | ARSB |
|
Lysosomal Storage Diseases (LSDs) | P15848 | |
CON00043 | Maroteaux-Lamy syndrome, mild form | ARSB |
|
Lysosomal Storage Diseases (LSDs) | P15848 | |
CON00044 | Maroteaux-Lamy syndrome, intermediate form | ARSB |
|
Lysosomal Storage Diseases (LSDs) | P15848 | |
CON00091 | Farber Lipogranulomatosis | ASAH1 |
|
Lysosomal Storage Diseases (LSDs) | Q13510 | |
CON00092 | Farber Lipogranulomatosis, type 1 | ASAH1 |
|
Lysosomal Storage Diseases (LSDs) | Q13510 | |
CON00093 | Farber Lipogranulomatosis, type 2 | ASAH1 |
|
Lysosomal Storage Diseases (LSDs) | Q13510 | |
CON00094 | Farber Lipogranulomatosis, type 3 | ASAH1 |
|
Lysosomal Storage Diseases (LSDs) | Q13510 | |
CON00095 | Farber Lipogranulomatosis, type 4 | ASAH1 |
|
Lysosomal Storage Diseases (LSDs) | Q13510 | |
CON00096 | Farber Lipogranulomatosis, type 5 | ASAH1 |
|
Lysosomal Storage Diseases (LSDs) | Q13510 | |
CON00371 | ATP6VOA2-CDG | ATP6V0A2 |
|
Congenital Disorders of Glycosylation (CDGs) | Q9Y487 |
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Last updated: August 19, 2024