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Glyco-Disease Genes Database (GDGDB)
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 | |
| CON00006 | Fucosidosis | FUCA1 |
|
Lysosomal Storage Diseases (LSDs) | P04066 | |
| CON00009 | Alpha-mannosidosis, type I (early-onset) | MAN2B1 |
|
Lysosomal Storage Diseases (LSDs) | O00754 | |
| CON00010 | Alpha-mannosidosis, type II (later-onset) | MAN2B1 |
|
Lysosomal Storage Diseases (LSDs) | O00754 | |
| CON00015 | Sialidosis type II, congenital form | NEU1 |
|
Lysosomal Storage Diseases (LSDs) | Q99519 | |
| CON00016 | Sialidosis type II, infantile form | NEU1 |
|
Lysosomal Storage Diseases (LSDs) | Q99519 | |
| CON00017 | Sialidosis type II, juvenile form | NEU1 |
|
Lysosomal Storage Diseases (LSDs) | Q99519 | |
| 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 | |
| CON00059 | Sandhoff disease, infantile form | HEXB |
|
Lysosomal Storage Diseases (LSDs) | P07686 | |
| CON00060 | Sandhoff disease, juvenile form | HEXB |
|
Lysosomal Storage Diseases (LSDs) | P07686 | |
| CON00061 | Sandhoff disease, adult form | HEXB |
|
Lysosomal Storage Diseases (LSDs) | P07686 | |
| CON00067 | Gaucher disease, type II | GBA |
|
Lysosomal Storage Diseases (LSDs) | P04062 | |
| CON00068 | Gaucher disease, type II, neuronopathic form, classic type | GBA |
|
Lysosomal Storage Diseases (LSDs) | P04062 | |
| CON00069 | Gaucher disease, type II, perinatal lethal form | GBA |
|
Lysosomal Storage Diseases (LSDs) | P04062 | |
| CON00072 | Gaucher disease, atypical, due to saposin C deficiency | PSAP |
|
Lysosomal Storage Diseases (LSDs) | P07602 | |
| CON00074 | Krabbe disease, infantile form | GALC |
|
Lysosomal Storage Diseases (LSDs) | P54803 | |
| CON00075 | Krabbe disease, late-onset form | GALC |
|
Lysosomal Storage Diseases (LSDs) | P54803 | |
| 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 | |
| CON00090 | Niemann-Pick disease, type C2 | NPC2 |
|
Lysosomal Storage Diseases (LSDs) | P61916 | |
| CON00092 | Farber Lipogranulomatosis, type 1 | ASAH1 |
|
Lysosomal Storage Diseases (LSDs) | Q13510 |
