GO Term |
---|
Golgi lumen |
lysosomal lumen |
extracellular region |
extracellular space |
collagen-containing extracellular matrix |
GO Term |
---|
RNA binding |
glycosaminoglycan binding |
extracellular matrix binding |
extracellular matrix structural constituent conferring compression resistance |
Position | Description | PubMed ID | GlyTouCan ID | Source |
---|---|---|---|---|
262 |
|
|
Pathway Name | Organism |
---|---|
A tetrasaccharide linker sequence is required for GAG synthesis | Homo sapiens |
CS/DS degradation | Homo sapiens |
Chondroitin sulfate biosynthesis | Homo sapiens |
Defective B3GALT6 causes EDSP2 and SEMDJL1 | Homo sapiens |
Defective B3GAT3 causes JDSSDHD | Homo sapiens |
Defective B4GALT7 causes EDS, progeroid type | Homo sapiens |
Defective CHST14 causes EDS, musculocontractural type | Homo sapiens |
Defective CHST3 causes SEDCJD | Homo sapiens |
Defective CHSY1 causes TPBS | Homo sapiens |
Degradation of the extracellular matrix | Homo sapiens |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:0110300 | obsolete autosomal dominant limb-girdle muscular dystrophy type 1A | |
DOID:0110301 | obsolete autosomal dominant limb-girdle muscular dystrophy type 1B | |
DOID:0110302 | obsolete autosomal dominant limb-girdle muscular dystrophy type 1C | |
DOID:0110303 | autosomal dominant limb-girdle muscular dystrophy type 1H | |
DOID:0110304 | autosomal dominant limb-girdle muscular dystrophy type 2 | |
DOID:0110305 | autosomal dominant limb-girdle muscular dystrophy type 1 | |
DOID:0110306 | autosomal dominant limb-girdle muscular dystrophy type 3 | |
DOID:0110334 | osteogenesis imperfecta type 1 | |
DOID:0110335 | osteogenesis imperfecta with opalescent teeth, blue sclerae and wormian bones but without fractures | |
DOID:0110336 | osteogenesis imperfecta type 8 |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
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Last updated: August 19, 2024