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    Data summary

    • Publications : 991
    • Phenotypes : 178
    • Genes : 207
    • Mutations : 4571
    • SNVs : 3402
    • InDels : 1169
    • Last Update : 26/10/2017

    Detailed information for MFRP






    Basic information
    Official symbolMFRP
    Official full namemembrane frizzled-related protein
    Location11q23
    Gene typeprotein-coding
    SynonymsMCOP5|NNO2|RD6
    Quick linksEntrez ID:83552; HGNC:18121; MIM:606227; Ensembl:ENSG00000235718; HPRD:ENSG00000259159; Vega:06941
    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:0048856anatomical structure development403010250.132.034.19e-161.33e-14
    GO:0032502developmental process457210456.881.833.53e-131.04e-11
    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
    chr11119208651119218383611040"Microphthalmia, isolated 5"360622711q23.3
    chr11119208651119218383609549Nanophthalmos 2360622711q23.3
    MGI related
    chromosomebeginendgene IDgene symbol of mouseMGIMPphenotype description
    chr1111920865111921838383552MfrpMGI:2385957MP:0001186pigmentation phenotype
    chr1111920865111921838383552MfrpMGI:2385957MP:0003631nervous system phenotype
    chr1111920865111921838383552MfrpMGI:2385957MP:0005391vision/eye phenotype
    Mutation spectrum

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    Gene-disease network

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