GO Term |
---|
Golgi lumen |
focal adhesion |
lysosomal lumen |
extracellular region |
basement membrane |
extracellular space |
plasma membrane |
axon |
collagen-containing extracellular matrix |
plasma membrane protein complex |
Position | Description | PubMed ID | GlyTouCan ID | Source |
---|---|---|---|---|
2151 |
|
|||
2160 |
|
|||
2161 |
|
|||
2223 |
|
|||
2429 |
|
|||
2524 |
|
|||
2525 |
|
|||
2529 |
|
|||
2541 |
|
|||
2559 |
|
Pathway Name | Organism |
---|---|
A tetrasaccharide linker sequence is required for GAG synthesis | Homo sapiens |
Amyloid fiber formation | Homo sapiens |
Attachment and Entry | 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 EXT1 causes exostoses 1, TRPS2 and CHDS | Homo sapiens |
Defective EXT2 causes exostoses 2 | Homo sapiens |
Degradation of the extracellular matrix | Homo sapiens |
ECM proteoglycans | Homo sapiens |
DO ID | Disease Name | Source |
---|---|---|
DOID:0060583 | Noonan syndrome 5 | |
DOID:0060584 | Noonan syndrome 6 | |
DOID:0060585 | Noonan syndrome 7 | |
DOID:0060586 | Noonan syndrome 8 | |
DOID:0060587 | Noonan syndrome 9 | |
DOID:0060588 | Noonan syndrome 10 | |
DOID:0060608 | microcephalic osteodysplastic primordial dwarfism type I | |
DOID:0060609 | microcephalic osteodysplastic primordial dwarfism type II | |
DOID:0060644 | chondrodysplasia-pseudohermaphroditism syndrome | |
DOID:0060673 | Peters anomaly |
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024