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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 GPR98






    Basic information
    Official symbolGPR98
    Official full nameG protein-coupled receptor 98
    Location5q13
    Gene typeprotein-coding
    SynonymsFEB4|MASS1|USH2B|USH2C|VLGR1|VLGR1b
    Quick linksEntrez ID:84059; HGNC:17416; MIM:602851; Ensembl:ENSG00000164199; HPRD:09111; Vega:OTTHUMG00000162668
    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:0045494photoreceptor cell maintenance25220.3170.747.36e-401.44e-37
    GO:0043954cellular component maintenance38220.4746.546.20e-338.09e-31
    GO:0007423sensory organ development436485.428.853.27e-323.84e-30
    GO:0009582detection of abiotic stimulus83271.0326.151.40e-311.49e-29
    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:0051606detection of stimulus202272.5110.742.10e-209.13e-19
    GO:0044699single-organism process768215295.571.599.26e-193.88e-17
    GO:0030030cell projection organization9344611.623.962.85e-169.84e-15
    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:0005509calcium ion binding668177.432.290.00130.0157
    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
    chr58985361690461033604352"Febrile seizures, familial, 4"36028515q14.3
    chr58985361690461033605472"Usher syndrome, type 2C"36028515q14.3
    chr58985361690461033605472"Usher syndrome, type 2C, GPR98/PDZD7 digenic"36028515q14.3
    MGI related
    chromosomebeginendgene IDgene symbol of mouseMGIMPphenotype description
    chr5898536169046103384059Gpr98MGI:1274784MP:0003631nervous system phenotype
    chr5898536169046103384059Gpr98MGI:1274784MP:0005377hearing/vestibular/ear phenotype
    chr5898536169046103384059Gpr98MGI:1274784MP:0005386behavior/neurological phenotype
    chr5898536169046103384059Gpr98MGI:1274784MP:0005391vision/eye phenotype
    chr5898536169046103384059Gpr98MGI:1274784MP:0010768mortality/aging
    Mutation spectrum

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    Gene-disease network

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