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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Syndecan-2
Summary
- UniProt ID
- P34741
- Gene Symbol
-
- SDC2
- HSPG1
- Organism
- Homo sapiens (human)
External Links
- GlyConnect
- GlyGen
- P34741
- PubChem
- P34741
- The Human Metabolome Database
- HMDBP10737
Annotation
- Keyword
-
- 3D-structure
- Differentiation
- Heparan sulfate
- Neurogenesis
- Phosphoprotein
- Reference proteome
- Signal
- Transmembrane helix
- Gene Ontology (GO)
| GO Term |
|---|
| cell migration |
| dendrite morphogenesis |
| regulation of dendrite morphogenesis |
| GO Term |
|---|
| endoplasmic reticulum lumen |
| Golgi lumen |
| cell surface |
| lysosomal lumen |
| plasma membrane |
| collagen-containing extracellular matrix |
| GO Term |
|---|
| PDZ domain binding |
| identical protein binding |
Sequence
MRRAWILLTLGLVACVSAESRAELTSDKDMYLDNSSIEEASGVYPIDDDDYASASGSGADEDVESPELTTSRPLPKILLTSAAPKVETTTLNIQNKIPAQTKSPEETDKEKVHLSDSERKMDPAEEDTNVYTEKHSDSLFKRTEVLAAVIAGGVIGFLFAIFLILLLVYRMRKKDEGSYDLGERKPSSAAYQKAPTKEFYA
Glycosylation Sites
G57321FI
G29931IJ
G43417UB
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 |
| EPHB-mediated forward signaling | Homo sapiens |
| HS-GAG biosynthesis | 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:0050156 | idiopathic pulmonary fibrosis | |
| DOID:0050453 | lissencephaly | |
| DOID:0050557 | congenital muscular dystrophy | |
| DOID:0050777 | Joubert syndrome | |
| DOID:0050788 | proximal symphalangism | |
| DOID:0050819 | obsolete Matthew-Wood syndrome | |
| DOID:0050865 | tongue squamous cell carcinoma | |
| DOID:0050894 | ameloblastoma | |
| DOID:0060180 | colitis | |
| DOID:0060189 | ileitis |
