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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 |
|---|
| plasma membrane |
| collagen-containing extracellular matrix |
| endoplasmic reticulum lumen |
| Golgi lumen |
| cell surface |
| lysosomal lumen |
| 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 |
|---|---|
| HS-GAG degradation | Homo sapiens |
| Post-translational protein phosphorylation | Homo sapiens |
| RSV-host interactions | Homo sapiens |
| Regulation of IGF Activity by IGFBP | Homo sapiens |
| Respiratory syncytial virus (RSV) attachment and entry | Homo sapiens |
| Retinoid metabolism and transport | Homo sapiens |
| Syndecan interactions | 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:0060190 | ileocolitis | |
| DOID:0060255 | rippling muscle disease 2 | |
| DOID:0060270 | pontocerebellar hypoplasia type 2D | |
| DOID:0060276 | pontocerebellar hypoplasia type 7 | |
| DOID:0060277 | pontocerebellar hypoplasia type 8 | |
| DOID:0060278 | pontocerebellar hypoplasia type 9 | |
| DOID:0060469 | Miller-Dieker lissencephaly syndrome | |
| DOID:0060807 | syndromic X-linked intellectual disability Najm type | |
| DOID:0070027 | CST3-related cerebral amyloid angiopathy | |
| DOID:0070247 | autosomal dominant Emery-Dreifuss muscular dystrophy 2 |
