HCSGD entry for VCAN


1. General information

Official gene symbolVCAN
Entrez ID1462
Gene full nameversican
Other gene symbolsCSPG2 ERVR GHAP PG-M WGN WGN1
Links to Entrez GeneLinks to Entrez Gene

2. Neighbors in the network

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This gene isn't in Literature mining network.

3. Gene ontology annotation

GO ID

GO term

Evidence

Category

GO:0005509Calcium ion bindingIEAmolecular_function
GO:0005515Protein bindingIPImolecular_function
GO:0005539Glycosaminoglycan bindingTASmolecular_function
GO:0005540Hyaluronic acid bindingIEAmolecular_function
GO:0005576Extracellular regionTAScellular_component
GO:0005578Proteinaceous extracellular matrixIEAcellular_component
GO:0005615Extracellular spaceIDAcellular_component
GO:0005796Golgi lumenTAScellular_component
GO:0005975Carbohydrate metabolic processTASbiological_process
GO:0007155Cell adhesionIEAbiological_process
GO:0007275Multicellular organismal developmentTASbiological_process
GO:0007507Heart developmentIEAbiological_process
GO:0008037Cell recognitionTASbiological_process
GO:0008347Glial cell migrationIDAbiological_process
GO:0030198Extracellular matrix organizationTASbiological_process
GO:0030203Glycosaminoglycan metabolic processTASbiological_process
GO:0030204Chondroitin sulfate metabolic processTASbiological_process
GO:0030206Chondroitin sulfate biosynthetic processTASbiological_process
GO:0030207Chondroitin sulfate catabolic processTASbiological_process
GO:0030208Dermatan sulfate biosynthetic processTASbiological_process
GO:0030246Carbohydrate bindingIEAmolecular_function
GO:0031012Extracellular matrixIDA ISScellular_component
GO:0043202Lysosomal lumenTAScellular_component
GO:0044281Small molecule metabolic processTASbiological_process
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.95687210590.00152792830.99999024730.0758803774

  • Individual experiment result
    ( "-" represent NA in the specific microarray platform )

Data sourceUp or downLog fold change
GSE11954Down-0.2865925805
GSE13712_SHEARDown-1.8159602543
GSE13712_STATICDown-0.7739201271
GSE19018Down-0.5375599155
GSE19899_A1Down-0.2703191743
GSE19899_A2Down-1.0986759817
PubMed_21979375_A1Down-1.1272451247
PubMed_21979375_A2Down-0.8852250439
GSE35957Up0.3247717462
GSE36640Down-0.2927938524
GSE54402Down-0.2227319925
GSE9593Down-1.6601697796
GSE43922Up0.1258017267
GSE24585Down-0.9059590623
GSE37065Down-0.1628778018
GSE28863_A1Up0.4434401697
GSE28863_A2Up0.3444262654
GSE28863_A3Down-0.0036709433
GSE28863_A4Down-0.3404977708
GSE48662Down-0.3776646096

5. Regulation relationships with compounds/drugs/microRNAs

  • Compounds

Not regulated by compounds

  • Drugs

Name

Drug

Accession number

Hyaluronic acidDB08818 -

  • MicroRNAs

  • mirTarBase
No target information from mirTarBase
  • mirRecord
No target information from mirRecord

6. Text-mining results about the gene

Gene occurances in abstracts of cellular senescence-associated articles: 1 abstracts the gene occurs.


PubMed ID of the article

Sentenece the gene occurs

19164294Versican/PG-M Assembles Hyaluronan into Extracellular Matrix and Inhibits CD44-mediated Signaling toward Premature Senescence in Embryonic Fibroblasts
19164294Versican/PG-M is a large chondroitin sulfate proteoglycan of the extracellular matrix which interacts with hyaluronan at the N-terminal G1 domain, composed of A, B, and B' subdomains
19164294Recently, we generated knock-in mice Cspg2(Delta3/Delta3), whose versican, without the A subdomain, has decreased hyaluronan (HA) binding affinity, thereby exhibiting reduced deposition of versican in the extracellular matrix
19164294Whereas the extracellular matrix of the wild type fibroblasts exhibited a network structure of hyaluronan and versican, that of the Cspg2(Delta3/Delta3) fibroblasts exhibited approximately 35 and approximately 85% deposition of versican and HA, without such a structure
19164294These results demonstrate that versican is essential for matrix assembly involving hyaluronan and that diminished versican deposition increases free hyaluronan fragments that interact with CD44 and increase phosphorylation of ERK1/2, leading to cellular senescence
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