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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 RGS9






    Basic information
    Official symbolRGS9
    Official full nameregulator of G-protein signaling 9
    Location17q24
    Gene typeprotein-coding
    SynonymsPERRS|RGS9L
    Quick linksEntrez ID:8787; HGNC:10004; MIM:604067; Ensembl:ENSG00000108370; HPRD:04962; Vega:OTTHUMG00000179349
    GO related
    GO term accessionGO term nameNumber of reference genesNumber of genesExpected numberRatio of enrichmentP-valueAdjusted P-Value
    GO:0050953sensory perception of light stimulus2051002.5539.218.72e-1461.02e-142
    GO:0007601visual perception204992.5439.017.39e-1444.34e-141
    GO:0007600sensory perception4951036.1616.734.54e-1051.78e-102
    GO:0050877neurological system process123710615.396.891.82e-665.34e-64
    GO:0003008system process169510821.095.121.12e-542.63e-52
    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: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:0044459plasma membrane part19184120.921.961.68e-059.98e-05
    Pathway related
    TermSurceNumber of reference genesNumber of genesExpected numberRatio of enrichmentP-valueAdjusted P-value
    Visual signal transduction: RodsPathway commons24170.11157.472.08e-352.14e-33
    Visual signal transduction: ConesPathway commons23150.10144.981.71e-308.81e-29
    PhototransductionKEGG29120.1391.992.36e-215.66e-20
    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
    chr176313245563224821608415Bradyopsia360406717q24.1
    chr176313245563224821608415Bradyopsia360781419q13.11
    MGI related
    chromosomebeginendgene IDgene symbol of mouseMGIMPphenotype description
    chr1763132455632248218787Rgs9MGI:1338824MP:0003631nervous system phenotype
    chr1763132455632248218787Rgs9MGI:1338824MP:0005386behavior/neurological phenotype
    chr1763132455632248218787Rgs9MGI:1338824MP:0005391vision/eye phenotype
    Mutation spectrum

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    Gene-disease network

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