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HSPG2
HPA
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  • HSPG2
PROTEIN SUMMARY GENE INFORMATION RNA DATA ANTIBODY DATA
GENERAL INFORMATIONi

General description of the gene and the encoded protein(s) using information from HGNC and Ensembl, as well as predictions made by the Human Protein Atlas project.

Gene namei

Official gene symbol, which is typically a short form of the gene name, according to HGNC.

HSPG2
Synonyms perlecan, PRCAN, SJS1
Gene descriptioni

Full gene name according to HGNC.

Heparan sulfate proteoglycan 2
Protein classi

Assigned HPA protein class(es) for the encoded protein(s).

Disease related genes
Human disease related genes
Plasma proteins
Predicted locationi

All transcripts of all genes have been analyzed regarding the location(s) of corresponding protein based on prediction methods for signal peptides and transmembrane regions.

  • Genes with at least one transcript predicted to encode a secreted protein, according to prediction methods or to UniProt location data, have been further annotated and classified with the aim to determine if the corresponding protein(s) are secreted or actually retained in intracellular locations or membrane-attached.

  • Remaining genes, with no transcript predicted to encode a secreted protein, will be assigned the prediction-based location(s).

The annotated location overrules the predicted location, so that a gene encoding a predicted secreted protein that has been annotated as intracellular will have intracellular as the final location.

Secreted, Intracellular
Protein evidence Evidence at protein level (all genes)
GENE INFORMATIONi

Gene information from Ensembl and Entrez, as well as links to available gene identifiers are displayed here. Information was retrieved from Ensembl if not indicated otherwise.

Chromosome 1
Cytoband p36.12
Chromosome location (bp) 21822244 - 21937310
Number of transcriptsi

Number of protein-coding transcripts from the gene as defined by Ensembl.

5
Ensembl ENSG00000142798 (version 109)
Entrez gene 3339
HGNC HGNC:5273
UniProt P98160 (UniProt - Evidence at protein level)
neXtProt NX_P98160
GeneCards HSPG2
Antibodypedia HSPG2 antibodies


PROTEIN FUNCTION
Protein function (UniProt)i

Useful information about the protein provided by UniProt.

Integral component of basement membranes. Component of the glomerular basement membrane (GBM), responsible for the fixed negative electrostatic membrane charge, and which provides a barrier which is both size- and charge-selective. It serves as an attachment substrate for cells. Plays essential roles in vascularization. Critical for normal heart development and for regulating the vascular response to injury. Also required for avascular cartilage development.... show less
Biological process (UniProt)i

Keywords assigned by UniProt to proteins because they are involved in a particular biological process.

Angiogenesis
Ligand (UniProt)i

Keywords assigned by UniProt to proteins because they bind, are associated with, or whose activity is dependent of some molecule.

Calcium, Metal-binding
Gene summary (Entrez)i

Useful information about the gene from Entrez

This gene encodes the perlecan protein, which consists of a core protein to which three long chains of glycosaminoglycans (heparan sulfate or chondroitin sulfate) are attached. The perlecan protein is a large multidomain proteoglycan that binds to and cross-links many extracellular matrix components and cell-surface molecules. It has been shown that this protein interacts with laminin, prolargin, collagen type IV, FGFBP1, FBLN2, FGF7 and transthyretin, etc., and it plays essential roles in multiple biological activities. Perlecan is a key component of the vascular extracellular matrix, where it helps to maintain the endothelial barrier function. It is a potent inhibitor of smooth muscle cell proliferation and is thus thought to help maintain vascular homeostasis. It can also promote growth factor (e.g., FGF2) activity and thus stimulate endothelial growth and re-generation. It is a major component of basement membranes, where it is involved in the stabilization of other molecules as well as being involved with glomerular permeability to macromolecules and cell adhesion. Mutations in this gene cause Schwartz-Jampel syndrome type 1, Silverman-Handmaker type of dyssegmental dysplasia, and tardive dyskinesia. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, May 2014]... show less
PROTEIN INFORMATIONi

The protein information section displays alternative protein-coding transcripts (splice variants) encoded by this gene according to the Ensembl database.

The Splice variant identifier links to the Ensembl website protein summary for the selected splice variant. The data in the Swissprot and TrEMBL columns links to corresponding pages in the UniProt database.

The protein classes assigned to this protein are shown if expanding the data in the protein class column. Parent protein classes are in bold font and subclasses are listed under the parent class.

The length of the protein (amino acid residues according to Ensembl), molecular mass (kDalton), predicted signal peptide and number of predicted transmembrane region(s) according to in-house majority decision methods based on sets of predictors are also reported.
Splice variant SwissProt TrEMBL Protein class Gene ontology Length & mass Signal peptide
(predicted)
Transmembrane regions
(predicted)
HSPG2-201
ENSP00000497688
ENST00000374673
A0A3B3IT11
[Direct mapping] Basement membrane-specific heparan sulfate proteoglycan core protein
Show all
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Human disease related genes
   Congenital malformations
   Congenital malformations of the musculoskeletal system
   Musculoskeletal diseases
   Muscular diseases
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0005515 [protein binding]
Show all
288 aa
31.5 kDa
No 0
HSPG2-202
ENSP00000363808
ENST00000374676
H7BYA5
[Direct mapping] Basement membrane-specific heparan sulfate proteoglycan core protein
Show all
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Human disease related genes
   Congenital malformations
   Congenital malformations of the musculoskeletal system
   Musculoskeletal diseases
   Muscular diseases
Protein evidence (Ezkurdia et al 2014)
Show all
109 aa
12 kDa
No 0
HSPG2-203
ENSP00000363827
ENST00000374695
P98160
[Direct mapping] Basement membrane-specific heparan sulfate proteoglycan core protein Endorepellin LG3 peptide
Show all
Predicted secreted proteins
   Secreted proteins predicted by MDSEC
   SignalP predicted secreted proteins
   Phobius predicted secreted proteins
   SPOCTOPUS predicted secreted proteins
   DeepTMHMM predicted secreted proteins
   DeepSig predicted secreted proteins
Plasma proteins
Disease related genes
Human disease related genes
   Congenital malformations
   Congenital malformations of the musculoskeletal system
   Musculoskeletal diseases
   Muscular diseases
Mapped to neXtProt
   neXtProt - Evidence at protein level
Protein evidence (Kim et al 2014)
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0001525 [angiogenesis]
GO:0001540 [amyloid-beta binding]
GO:0005509 [calcium ion binding]
GO:0005515 [protein binding]
GO:0005576 [extracellular region]
GO:0005604 [basement membrane]
GO:0005615 [extracellular space]
GO:0005796 [Golgi lumen]
GO:0005886 [plasma membrane]
GO:0005925 [focal adhesion]
GO:0006629 [lipid metabolic process]
GO:0006898 [receptor-mediated endocytosis]
GO:0006954 [inflammatory response]
GO:0007420 [brain development]
GO:0008022 [protein C-terminus binding]
GO:0009887 [animal organ morphogenesis]
GO:0009888 [tissue development]
GO:0016525 [negative regulation of angiogenesis]
GO:0030021 [extracellular matrix structural constituent conferring compression resistance]
GO:0030154 [cell differentiation]
GO:0043202 [lysosomal lumen]
GO:0046872 [metal ion binding]
GO:0050750 [low-density lipoprotein particle receptor binding]
GO:0062023 [collagen-containing extracellular matrix]
GO:0070062 [extracellular exosome]
GO:0071944 [cell periphery]
GO:0072359 [circulatory system development]
GO:0098797 [plasma membrane protein complex]
Show all
4391 aa
468.8 kDa
Yes 0
HSPG2-214
ENSP00000489161
ENST00000635682
A0A0U1RQT3
[Direct mapping] Basement membrane-specific heparan sulfate proteoglycan core protein
Show all
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Human disease related genes
   Congenital malformations
   Congenital malformations of the musculoskeletal system
   Musculoskeletal diseases
   Muscular diseases
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0005509 [calcium ion binding]
Show all
307 aa
33.3 kDa
No 0
HSPG2-215
ENSP00000496473
ENST00000644714
A0A2R8YH07
[Direct mapping] Basement membrane-specific heparan sulfate proteoglycan core protein
Show all
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Human disease related genes
   Congenital malformations
   Congenital malformations of the musculoskeletal system
   Musculoskeletal diseases
   Muscular diseases
Protein evidence (Ezkurdia et al 2014)
Show all
236 aa
25.7 kDa
No 0

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