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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 TRIM32






    Basic information
    Official symbolTRIM32
    Official full nametripartite motif containing 32
    Location9q33.1
    Gene typeprotein-coding
    SynonymsBBS11|HT2A|LGMD2H|TATIP
    Quick linksEntrez ID:22954; HGNC:16380; MIM:602290; Ensembl:ENSG00000119401; HPRD:03797; Vega:OTTHUMG00000021026
    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:0009416response to light stimulus203292.5311.481.06e-225.41e-21
    GO:0044699single-organism process768215295.571.599.26e-193.88e-17
    GO:0009314response to radiation319293.977.313.46e-171.35e-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
    GO:0017022myosin binding2930.329.300.00400.0304
    GO:0044430cytoskeletal part12873914.042.783.99e-093.91e-08
    GO:0005856cytoskeleton17904719.522.417.23e-096.16e-08
    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
    chr9119448580119464579209900Bardet-Biedl syndrome 1136022909q33.1
    chr9119448580119464579254110"Muscular dystrophy, limb-girdle, type 2H"36022909q33.1
    MGI related
    chromosomebeginendgene IDgene symbol of mouseMGIMPphenotype description
    chr911944858011946457922954Trim32MGI:1917057MP:0003631nervous system phenotype
    chr911944858011946457922954Trim32MGI:1917057MP:0005369muscle phenotype
    chr911944858011946457922954Trim32MGI:1917057MP:0005376homeostasis/metabolism phenotype
    chr911944858011946457922954Trim32MGI:1917057MP:0005378growth/size phenotype
    chr911944858011946457922954Trim32MGI:1917057MP:0005386behavior/neurological phenotype
    chr911944858011946457922954Trim32MGI:1917057MP:0005389reproductive system phenotype
    Mutation spectrum

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    Gene-disease network

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