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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 OPN1MW






    Basic information
    Official symbolOPN1MW
    Official full nameopsin 1 (cone pigments), medium-wave-sensitive
    LocationXq28
    Gene typeprotein-coding
    SynonymsCBBM|CBD|COD5|GCP|GOP|OPN1MW1
    Quick linksEntrez ID:2652; HGNC:4206; MIM:300821; Ensembl:02365; HPRD:; Vega:
    GO related
    GO term accessionGO term nameNumber of reference genesNumber of genesExpected numberRatio of enrichmentP-valueAdjusted P-Value
    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_56630.0648.692.08e-050.0004
    Hsapiens_Module_912751.303.830.01000.0350
    OMIM related
    chromosomebeginenddisorder MIM numberdisorderphene mapping keygene/locus MIM numbercytogenetic loaction
    chrX153484202153500470303700Blue cone monochromacy3300821Xq28
    chrX153484202153500470303800"Colorblindness, deutan"3300821Xq28
    MGI related
    chromosomebeginendgene IDgene symbol of mouseMGIMPphenotype description
    chrX1534842021535004702652Opn1mwMGI:1097692MP:0005391vision/eye phenotype
    Mutation spectrum

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    Gene-disease network

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