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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 WDR19






    Basic information
    Official symbolWDR19
    Official full nameWD repeat domain 19
    Location4p14
    Gene typeprotein-coding
    SynonymsATD5|CED4|DYF-2|IFT144|NPHP13|ORF26|Oseg6|PWDMP
    Quick linksEntrez ID:57728; HGNC:18340; MIM:608151; Ensembl:ENSG00000157796; HPRD:10489; Vega:OTTHUMG00000160466
    GO related
    GO term accessionGO term nameNumber of reference genesNumber of genesExpected numberRatio of enrichmentP-valueAdjusted P-Value
    GO:0030030cell projection organization9344611.623.962.85e-169.84e-15
    GO:0005929cilium239552.6121.102.59e-585.08e-56
    GO:0031513nonmotile primary cilium80320.8736.671.40e-421.37e-40
    GO:0072372primary cilium96331.0531.522.93e-411.91e-39
    GO:0042995cell projection12306713.424.995.15e-302.02e-28
    GO:0005932microtubule basal body66200.7227.785.27e-241.48e-22
    GO:0044463cell projection part639426.976.032.11e-215.17e-20
    GO:0032391photoreceptor connecting cilium23120.2547.832.41e-184.72e-17
    GO:0005815microtubule organizing center486315.305.851.61e-152.87e-14
    GO:0015630microtubule cytoskeleton863379.413.935.76e-138.68e-12
    GO:0044430cytoskeletal part12873914.042.783.99e-093.91e-08
    GO:0005856cytoskeleton17904719.522.417.23e-096.16e-08
    GO:0031514motile cilium1250.1338.201.09e-078.90e-07
    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
    chr43918302339288430614376Asphyxiating thoracic dystrophy 536081514p14
    chr43918302339288430614378Cranioectodermal dysplasia 436081514p14
    chr43918302339288430614377Nephronophthisis 1336081514p14
    MGI related
    chromosomebeginendgene IDgene symbol of mouseMGIMPphenotype description
    chr4391830233928843057728Wdr19MGI:2443231MP:0003631nervous system phenotype
    chr4391830233928843057728Wdr19MGI:2443231MP:0005369muscle phenotype
    chr4391830233928843057728Wdr19MGI:2443231MP:0005371limbs/digits/tail phenotype
    chr4391830233928843057728Wdr19MGI:2443231MP:0005377hearing/vestibular/ear phenotype
    chr4391830233928843057728Wdr19MGI:2443231MP:0005380embryogenesis phenotype
    chr4391830233928843057728Wdr19MGI:2443231MP:0005381digestive/alimentary phenotype
    chr4391830233928843057728Wdr19MGI:2443231MP:0005382craniofacial phenotype
    chr4391830233928843057728Wdr19MGI:2443231MP:0005384cellular phenotype
    chr4391830233928843057728Wdr19MGI:2443231MP:0005390skeleton phenotype
    chr4391830233928843057728Wdr19MGI:2443231MP:0005391vision/eye phenotype
    chr4391830233928843057728Wdr19MGI:2443231MP:0010768mortality/aging
    Mutation spectrum

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    Gene-disease network

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