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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 FAM161A






    Basic information
    Official symbolFAM161A
    Official full namefamily with sequence similarity 161, member A
    Location2p15
    Gene typeprotein-coding
    SynonymsRP28
    Quick linksEntrez ID:84140; HGNC:25808; MIM:613596; Ensembl:ENSG00000170264; HPRD:OTTHUMG00000152165; Vega:
    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:0005488binding11955150132.971.130.00050.0090
    GO:0031513nonmotile primary cilium80320.8736.671.40e-421.37e-40
    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
    Hsapiens_Module_26697167.162.240.00220.0114
    OMIM related
    chromosomebeginenddisorder MIM numberdisorderphene mapping keygene/locus MIM numbercytogenetic loaction
    chr26205098262082278606068Retinitis pigmentosa 2836135962p15
    MGI related
    chromosomebeginendgene IDgene symbol of mouseMGIMPphenotype description
    chr2620509826208227884140Fam161aMGI:1921123--
    Mutation spectrum

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    Gene-disease network

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