GO Term |
---|
extracellular exosome |
apical plasma membrane |
lamellipodium membrane |
ruffle |
nucleoplasm |
Golgi lumen |
focal adhesion |
cell surface |
lysosomal lumen |
extracellular region |
GO Term |
---|
protein kinase binding |
coreceptor activity |
Position | Description | PubMed ID | GlyTouCan ID | Source |
---|---|---|---|---|
130 | N-linked (GlcNAc...) asparagine |
|
||
348 | N-linked (GlcNAc...) asparagine | |||
427 | N-linked (GlcNAc...) asparagine |
|
||
685 | N-linked (GlcNAc...) asparagine | |||
772 | N-linked (GlcNAc...) asparagine | |||
995 | O-linked (Xyl...) (chondroitin sulfate) serine |
|
||
1131 | N-linked (GlcNAc...) asparagine | |||
1160 |
|
|||
1202 | N-linked (GlcNAc...) asparagine | |||
1364 | N-linked (GlcNAc...) asparagine |
|
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 |
Dermatan sulfate biosynthesis | Homo sapiens |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:0050558 | Ullrich congenital muscular dystrophy | |
DOID:0050848 | obstructive sleep apnea | |
DOID:0060180 | colitis | |
DOID:0060189 | ileitis | |
DOID:0060190 | ileocolitis | |
DOID:0080147 | lymphoblastic lymphoma | |
DOID:0080348 | Alzheimer's disease 1 | |
DOID:0110035 | Alzheimer's disease 2 | |
DOID:0110037 | Alzheimer's disease 5 | |
DOID:0110038 | Alzheimer's disease 6 |
GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
This work is licensed under Creative Commons Attribution 4.0 International
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Last updated: August 19, 2024