GO Term |
---|
extracellular region |
basement membrane |
extracellular space |
plasma membrane |
axon |
Golgi lumen |
focal adhesion |
lysosomal lumen |
collagen-containing extracellular matrix |
plasma membrane protein complex |
Position | Description | PubMed ID | GlyTouCan ID | Source |
---|---|---|---|---|
28 |
|
|||
40 |
|
|||
42 | O-linked (GalNAc...) threonine | |||
49 |
|
|||
52 |
|
|
||
65 | O-linked (Xyl...) (heparan sulfate) serine |
|
||
71 | O-linked (Xyl...) (heparan sulfate) serine |
|
||
76 | O-linked (Xyl...) (heparan sulfate) serine |
|
||
89 | N-linked (GlcNAc...) asparagine |
|
||
210 |
|
|
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:0050185 | erythema multiforme | |
DOID:0050426 | Stevens-Johnson syndrome | |
DOID:0050453 | lissencephaly | |
DOID:0050569 | Seckel syndrome | |
DOID:0050663 | Bethlem myopathy | |
DOID:0050741 | alcohol dependence | |
DOID:0050759 | myotonic dystrophy type 2 | |
DOID:0050766 | choreaacanthocytosis | |
DOID:0050777 | Joubert syndrome | |
DOID:0050788 | proximal symphalangism |
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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