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Glycan Structure Repository
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Glycoconjugate Repository
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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 ▲ |
|---|---|---|---|---|---|---|
| CON00045 | Mucopolysaccharidosis VII | GUSB |
|
Lysosomal Storage Diseases (LSDs) | P08236 | |
| CON00064 | Fabry disease | GLA |
|
Lysosomal Storage Diseases (LSDs) | P06280 | |
| CON00006 | Fucosidosis | FUCA1 |
|
Lysosomal Storage Diseases (LSDs) | P04066 | |
| CON00395 | Diastrophic dysplasia | SLC26A2 |
|
Congenital Disorders of Glycosylation (CDGs) | P50443 | |
| CON00067 | Gaucher disease, type II | GBA |
|
Lysosomal Storage Diseases (LSDs) | P04062 | |
| CON00391 | Macular corneal dystrophy | CHST6 |
|
Congenital Disorders of Glycosylation (CDGs) | Q9GZX3 | |
| CON00103 | Pompe disease | GAA |
|
Lysosomal Storage Diseases (LSDs) | P10253 | |
| CON00104 | Pompe disease, infantile-onset form | GAA |
|
Lysosomal Storage Diseases (LSDs) | P10253 | |
| CON00105 | Pompe disease, late-onset form | GAA |
|
Lysosomal Storage Diseases (LSDs) | P10253 | |
| CON00055 | Tay-Sachs disease | HEXA |
|
Lysosomal Storage Diseases (LSDs) | P06865 | |
| CON00056 | Tay-Sachs disease, infantile form | HEXA |
|
Lysosomal Storage Diseases (LSDs) | P06865 | |
| CON00057 | Tay-Sachs disease, late-onset forms | HEXA |
|
Lysosomal Storage Diseases (LSDs) | P06865 | |
| CON00058 | Sandhoff disease | HEXB |
|
Lysosomal Storage Diseases (LSDs) | P07686 | |
| 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 | |
| CON00012 | Sialidosis | NEU1 |
|
Lysosomal Storage Diseases (LSDs) | Q99519 | |
| CON00013 | Sialidosis type I | NEU1 |
|
Lysosomal Storage Diseases (LSDs) | Q99519 | |
| CON00014 | Sialidosis type II | NEU1 |
|
Lysosomal Storage Diseases (LSDs) | Q99519 | |
| 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 | |
| CON00008 | Alpha-mannosidosis | MAN2B1 |
|
Lysosomal Storage Diseases (LSDs) | O00754 | |
| 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 |
