GDGDB is a database of glycan-related diseases and their responsible genes.
Database | Last Updated |
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Glyco-Disease Genes Database (GDGDB) | January 25, 2017 |
Concept UI | Disease Name | Gene Symbol ▲ | Disease Name Aliases | Disease Type | UniProt ID | Disease IDs |
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Sialidosis type II, congenital form
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NEU1
|
Lysosomal Storage Diseases (LSDs)
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Sialidosis type II, infantile form
|
NEU1
|
Lysosomal Storage Diseases (LSDs)
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Sialidosis type II, juvenile form
|
NEU1
|
Lysosomal Storage Diseases (LSDs)
|
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Niemann-Pick disease, type C1
|
NPC1
|
|
Lysosomal Storage Diseases (LSDs)
|
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Niemann-Pick disease, type C2
|
NPC2
|
Lysosomal Storage Diseases (LSDs)
|
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Spondyloepimetaphyseal dysplasia, pakistani type
|
PAPSS2
|
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Congenital Disorders of Glycosylation (CDGs)
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PGM1-CDG
|
PGM1
|
|
Congenital Disorders of Glycosylation (CDGs)
|
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Paroxysmal nocturnal hemoglobinuria, somatic (SOMATIC MUTATION)
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PIGA
|
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Congenital Disorders of Glycosylation (CDGs)
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PIGM-CDG
|
PIGM
|
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Congenital Disorders of Glycosylation (CDGs)
|
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Multiple congenital anomalies-hypotonia-seizures syndrome 1
|
PIGN
|
|
Congenital Disorders of Glycosylation (CDGs)
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Partly supported by NIH Common Fund Grant #1U01GM125267-01