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GlyTouCan
Glycan Structure Repository
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Glycoconjugate Repository
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Glycomics MS raw data Repository
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Glycomics MS Repository for glycan annotations from GlycoWorkbench
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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Syndecan-1
Summary
- UniProt ID
- P18827
- Gene Symbol
-
- SDC1
- SDC
- Organism
- Homo sapiens (human)
External Links
- GlyGen
- P18827
- PubChem
- P18827
- The Human Metabolome Database
- HMDBP02143
- The O-GlcNAc Database
- P18827
- O-GlcNAcAtlas
- P18827
Annotation
- Keyword
-
- 3D-structure
- Heparan sulfate
- Phosphoprotein
- Reference proteome
- Secreted
- Signal
- Transmembrane helix
- Gene Ontology (GO)
| GO Term |
|---|
| response to glucocorticoid |
| response to calcium ion |
| striated muscle cell development |
| Sertoli cell development |
| GO Term |
|---|
| extracellular exosome |
| Golgi lumen |
| external side of plasma membrane |
| cell surface |
| lysosomal lumen |
| plasma membrane |
| protein-containing complex |
| GO Term |
|---|
| identical protein binding |
| cargo receptor activity |
Sequence
MRRAALWLWLCALALSLQPALPQIVATNLPPEDQDGSGDDSDNFSGSGAGALQDITLSQQTPSTWKDTQLLTAIPTSPEPTGLEATAASTSTLPAGEGPKEGEAVVLPEVEPGLTAREQEATPRPRETTQLPTTHLASTTTATTAQEPATSHPHRDMQPGHHETSTPAGPSQADLHTPHTEDGGPSATERAAEDGASSQLPAAEGSGEQDFTFETSGENTAVVAVEPDRRNQSPVDQGATGASQGLLDRKEVLGGVIAGGLVGLIFAVCLVGFMLYRMKKKDEGSYSLEEPKQANGGAYQKPTKQEEFYA
Glycosylation Sites
| Position | Description | PubMed ID | GlyTouCan ID | Source |
|---|---|---|---|---|
| 156 |
|
|||
| 164 |
|
|||
| 165 |
|
|||
| 166 |
|
|||
| 171 |
|
|||
| 177 |
|
|||
| 180 |
|
|||
| 186 |
|
|||
| 188 |
|
|||
| 197 |
|
G57321FI
G73004SD
G58001LT
G43417UB
G29068FM
Feature
: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt
Pathway
| Pathway Name | Organism |
|---|---|
| A tetrasaccharide linker sequence is required for GAG synthesis | Homo sapiens |
| Attachment and Entry | Homo sapiens |
| Cell surface interactions at the vascular wall | 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 |
| HS-GAG biosynthesis | Homo sapiens |
| HS-GAG degradation | Homo sapiens |
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
Disease
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0080334 | aortic valve disease 2 | |
| DOID:0080356 | IgG4-related disease | |
| DOID:0080531 | dedifferentiated liposarcoma | |
| DOID:0110115 | autoimmune lymphoproliferative syndrome type 2A | |
| DOID:0110116 | autoimmune lymphoproliferative syndrome type 2B | |
| DOID:0110119 | autoimmune lymphoproliferative syndrome type 3 | |
| DOID:0110425 | dilated cardiomyopathy 1A | |
| DOID:0110594 | primary ciliary dyskinesia 1 | |
| DOID:0110892 | inflammatory bowel disease 1 | |
| DOID:10283 | prostate cancer |
