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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Temtamy preaxial brachydactyly syndrome
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CHSY1
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Congenital Disorders of Glycosylation (CDGs)
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Spondyloepiphyseal dysplasia with congenital joint dislocations
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CHST3
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Congenital Disorders of Glycosylation (CDGs)
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Metachromatic leukodystrophy, due to saposin B deficiency
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PSAP
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Lysosomal Storage Diseases (LSDs)
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LFNG-CDG
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LFNG
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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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Niemann-Pick disease, type C1
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NPC1
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Lysosomal Storage Diseases (LSDs)
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POMT1/POMT2-CDG (cong. muscular dystrophy spectrum)
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POMT1,POMT2
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Congenital Disorders of Glycosylation (CDGs)
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POMGNT1-CDG (cong. muscular dystrophy spectrum)
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POMGNT1
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Congenital Disorders of Glycosylation (CDGs)
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Sialidosis
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NEU1
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Lysosomal Storage Diseases (LSDs)
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TUSC3-CDG
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TUSC3
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Congenital Disorders of Glycosylation (CDGs)
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01