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heparan sulfate proteoglycan 2
Summary
- Gene Symbol
-
- HSPG2
- Aliases
-
- PRCAN
- endorepellin
- perlecan
- perlecan proteoglycan
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Angiogenesis
- Basement membrane
- Calcium
- Direct protein sequencing
- Disease variant
- Disulfide bond
- EGF-like domain
- Heparan sulfate
- Immunoglobulin domain
- Laminin EGF-like domain
- Metal-binding
- Reference proteome
- Repeat
- Signal
- Proteins
| UniProt | Protein Name |
|---|---|
| P98160 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| animal organ regeneration | ||
| brain development |
|
|
| response to xenobiotic stimulus | ||
| angiogenesis | ||
| positive regulation of endothelial cell proliferation |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| extracellular region | ||
| Golgi lumen |
|
|
| basement membrane |
|
|
| plasma membrane |
|
|
| focal adhesion |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| collagen V binding |
GO Hierarchy
KEGG BRITE Database
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0080202 | adenoid cystic carcinoma | |
| DOID:0080348 | Alzheimer's disease 1 | |
| DOID:0080362 | X-linked spondyloepiphyseal dysplasia tarda | |
| DOID:0080390 | nephrotic syndrome type 1 | |
| DOID:0090005 | Schwartz-Jampel syndrome 1 | |
| DOID:0090032 | Silverman-Handmaker type dyssegmental dysplasia | |
| DOID:0090132 | complex cortical dysplasia with other brain malformations 7 | |
| DOID:0090137 | complex cortical dysplasia with other brain malformations 1 | |
| DOID:0110035 | Alzheimer's disease 2 | |
| DOID:0110037 | Alzheimer's disease 5 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000252 | Microcephaly |
| HP:0000270 | Delayed cranial suture closure |
| HP:0000272 | Malar flattening |
| HP:0000286 | Epicanthus |
| HP:0000293 | Full cheeks |
| HP:0000294 | Low anterior hairline |
| HP:0000298 | Mask-like facies |
| HP:0000307 | Pointed chin |
| HP:0000316 | Hypertelorism |
| HP:0000343 | Long philtrum |
| Disease ID | Disease Name |
|---|---|
| ORPHA:1606 |
|
| ORPHA:800 |
|
| ORPHA:1865 |
|
| OMIM:255800 |
|
| OMIM:224410 |
|
PubChem Disease
- GHR Health Conditions
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 175126 | WB:WBGene00006787 | ||
| 45320 | FB:FBgn0284408 | ||
| 565429 | ZFIN:ZDB-GENE-080807-4 | DANRE24960 | |
| 100380784 | SALSA43220 | ||
| 115165633 | SALTR88020 | ||
| 103467813 | POERE30093 | ||
| 102290874 | HAPBU05628 | ||
| 113013483 | ASTCA20652 | ||
| 108696836 | Xenbase:XB-GENE-17341349 | ||
| 100494785 | Xenbase:XB-GENE-6465357 |
