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    Data summary

    • Publications : 1001
    • Phenotypes : 178
    • Genes : 207
    • Mutations : 4631
    • SNVs : 3422
    • InDels : 1209
    • Last Update : 22/02/2019

    Detailed information for KLHL7






    Basic information
    Official symbolKLHL7
    Official full namekelch-like family member 7
    Location7p15.3
    Gene typeprotein-coding
    SynonymsKLHL6|SBBI26
    Quick linksEntrez ID:55975; HGNC:15646; MIM:611119; Ensembl:ENSG00000122550; HPRD:13927; Vega:OTTHUMG00000094813
    GO related
    GO term accessionGO term nameNumber of reference genesNumber of genesExpected numberRatio of enrichmentP-valueAdjusted P-Value
    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
    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
    chr72314435223216038612943Retinitis pigmentosa 4236111197p15.3
    MGI related
    chromosomebeginendgene IDgene symbol of mouseMGIMPphenotype description
    chr7231443522321603855975Klhl7MGI:1196453--
    Mutation spectrum

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    Gene-disease network

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