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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 PEX7






    Basic information
    Official symbolPEX7
    Official full nameperoxisomal biogenesis factor 7
    Location6q23.3
    Gene typeprotein-coding
    SynonymsPBD9B|PTS2R|RCDP1|RD
    Quick linksEntrez ID:5191; HGNC:8860; MIM:601757; Ensembl:ENSG00000112357; HPRD:03454; Vega:OTTHUMG00000015650
    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:0048856anatomical structure development403010250.132.034.19e-161.33e-14
    GO:0032502developmental process457210456.881.833.53e-131.04e-11
    GO:0005488binding11955150132.971.130.00050.0090
    GO:0005515protein binding733710281.611.250.00110.0149
    Pathway related
    TermSurceNumber of reference genesNumber of genesExpected numberRatio of enrichmentP-valueAdjusted P-value
    PeroxisomeKEGG7950.3614.073.01e-050.0002
    PPI related
    IDNumber of reference genesNumber of genesExpected numberRatio of enrichmentP-valueAdjusted P-value
    Hsapiens_Module_4631320.1314.980.00760.0304
    OMIM related
    chromosomebeginenddisorder MIM numberdisorderphene mapping keygene/locus MIM numbercytogenetic loaction
    chr6137142701137236072614879Peroxisome biogenesis disorder 9B36017576q23.3
    chr6137142701137236072215100"Rhizomelic chondrodysplasia punctata, type 1"36017576q23.3
    MGI related
    chromosomebeginendgene IDgene symbol of mouseMGIMPphenotype description
    chr61371427011372360725191Pex7MGI:1321392MP:0003631nervous system phenotype
    chr61371427011372360725191Pex7MGI:1321392MP:0005369muscle phenotype
    chr61371427011372360725191Pex7MGI:1321392MP:0005370liver/biliary system phenotype
    chr61371427011372360725191Pex7MGI:1321392MP:0005376homeostasis/metabolism phenotype
    chr61371427011372360725191Pex7MGI:1321392MP:0005378growth/size phenotype
    chr61371427011372360725191Pex7MGI:1321392MP:0005379endocrine/exocrine gland phenotype
    chr61371427011372360725191Pex7MGI:1321392MP:0005384cellular phenotype
    chr61371427011372360725191Pex7MGI:1321392MP:0005385cardiovascular system phenotype
    chr61371427011372360725191Pex7MGI:1321392MP:0005386behavior/neurological phenotype
    chr61371427011372360725191Pex7MGI:1321392MP:0005387immune system phenotype
    chr61371427011372360725191Pex7MGI:1321392MP:0005389reproductive system phenotype
    chr61371427011372360725191Pex7MGI:1321392MP:0005390skeleton phenotype
    chr61371427011372360725191Pex7MGI:1321392MP:0005391vision/eye phenotype
    chr61371427011372360725191Pex7MGI:1321392MP:0005397hematopoietic system phenotype
    chr61371427011372360725191Pex7MGI:1321392MP:0010768mortality/aging
    Mutation spectrum

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    Gene-disease network

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