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    Data summary

    • Publications : 991
    • Phenotypes : 178
    • Genes : 207
    • Mutations : 4583
    • SNVs : 3411
    • InDels : 1172
    • Last Update : 05/11/2017

    Detailed information for VCAN






    Basic information
    Official symbolVCAN
    Official full nameversican
    Location5q14.3
    Gene typeprotein-coding
    SynonymsCSPG2|ERVR|GHAP|PG-M|WGN|WGN1
    Quick linksEntrez ID:1462; HGNC:2464; MIM:118661; Ensembl:ENSG00000038427; HPRD:00340; Vega:OTTHUMG00000131321
    GO related
    GO term accessionGO term nameNumber of reference genesNumber of genesExpected numberRatio of enrichmentP-valueAdjusted P-Value
    GO:0044707single-multicellular organism process561214369.812.059.21e-297.72e-27
    GO:0032501multicellular organismal process564414370.212.041.83e-281.43e-26
    GO:0044699single-organism process768215295.571.599.26e-193.88e-17
    GO:0048646anatomical structure formation involved in morphogenesis15946219.833.134.32e-171.64e-15
    GO:0009653anatomical structure morphogenesis20557025.562.741.99e-167.08e-15
    GO:0030030cell projection organization9344611.623.962.85e-169.84e-15
    GO:0048856anatomical structure development403010250.132.034.19e-161.33e-14
    GO:0000902cell morphogenesis9454211.763.572.49e-137.69e-12
    GO:0032502developmental process457210456.881.833.53e-131.04e-11
    GO:0005488binding11955150132.971.130.00050.0090
    GO:0005509calcium ion binding668177.432.290.00130.0157
    GO:0005578proteinaceous extracellular matrix360143.933.574.22e-050.0002
    GO:0031012extracellular matrix426154.653.236.94e-050.0004
    Pathway related
    TermSurceNumber of reference genesNumber of genesExpected numberRatio of enrichmentP-valueAdjusted P-value
    PPI related
    IDNumber of reference genesNumber of genesExpected numberRatio of enrichmentP-valueAdjusted P-value
    OMIM related
    chromosomebeginenddisorder MIM numberdisorderphene mapping keygene/locus MIM numbercytogenetic loaction
    chr58276649282879122143200Wagner syndrome 131186615q14.2-q14.3
    MGI related
    chromosomebeginendgene IDgene symbol of mouseMGIMPphenotype description
    chr582766492828791221462VcanMGI:102889MP:0002873normal phenotype
    chr582766492828791221462VcanMGI:102889MP:0003631nervous system phenotype
    chr582766492828791221462VcanMGI:102889MP:0005371limbs/digits/tail phenotype
    chr582766492828791221462VcanMGI:102889MP:0005378growth/size phenotype
    chr582766492828791221462VcanMGI:102889MP:0005380embryogenesis phenotype
    chr582766492828791221462VcanMGI:102889MP:0005385cardiovascular system phenotype
    chr582766492828791221462VcanMGI:102889MP:0005390skeleton phenotype
    chr582766492828791221462VcanMGI:102889MP:0010768mortality/aging
    Mutation spectrum

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    Gene-disease network

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