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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 GRM6






    Basic information
    Official symbolGRM6
    Official full nameglutamate receptor, metabotropic 6
    Location5q35
    Gene typeprotein-coding
    SynonymsCSNB1B|GPRC1F|MGLUR6|mGlu6
    Quick linksEntrez ID:2916; HGNC:4598; MIM:604096; Ensembl:ENSG00000113262; HPRD:04975; Vega:
    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:0060041retina development in camera-type eye105311.3123.731.13e-341.90e-32
    GO:0009583detection of light stimulus47240.5841.054.99e-347.32e-32
    GO:0007423sensory organ development436485.428.853.27e-323.84e-30
    GO:0009582detection of abiotic stimulus83271.0326.151.40e-311.49e-29
    GO:0001654eye development276393.4311.363.01e-302.94e-28
    GO:0009581detection of external stimulus100271.2421.704.42e-293.99e-27
    GO:0044707single-multicellular organism process561214369.812.059.21e-297.72e-27
    GO:0032501multicellular organismal process564414370.212.041.83e-281.43e-26
    GO:0009584detection of visible light22160.2758.461.18e-267.70e-25
    GO:0043010camera-type eye development237332.9511.192.13e-251.25e-23
    GO:0009416response to light stimulus203292.5311.481.06e-225.41e-21
    GO:0051606detection of stimulus202272.5110.742.10e-209.13e-19
    GO:0044699single-organism process768215295.571.599.26e-193.88e-17
    GO:0009314response to radiation319293.977.313.46e-171.35e-15
    GO:0048856anatomical structure development403010250.132.034.19e-161.33e-14
    GO:0032502developmental process457210456.881.833.53e-131.04e-11
    GO:0044459plasma membrane part19184120.921.961.68e-059.98e-05
    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_912751.303.830.01000.0350
    Hsapiens_Module_2501620.1612.170.01140.0370
    OMIM related
    chromosomebeginenddisorder MIM numberdisorderphene mapping keygene/locus MIM numbercytogenetic loaction
    chr5178404329178423124257270"Night blindness, congenital stationary (complete), 1B, autosomal recessive"36040965q35.3
    MGI related
    chromosomebeginendgene IDgene symbol of mouseMGIMPphenotype description
    chr51784043291784231242916Grm6MGI:1351343MP:0003631nervous system phenotype
    chr51784043291784231242916Grm6MGI:1351343MP:0005386behavior/neurological phenotype
    chr51784043291784231242916Grm6MGI:1351343MP:0005391vision/eye phenotype
    Mutation spectrum

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    Gene-disease network

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