Quick Search:

  • Top 5 genes

    Top 5 diseases

    Data summary

    • Publications : 1001
    • Phenotypes : 178
    • Genes : 207
    • Mutations : 4631
    • SNVs : 3422
    • InDels : 1209
    • Last Update : 22/02/2019

    Detailed information for SDCCAG8






    Basic information
    Official symbolSDCCAG8
    Official full nameserologically defined colon cancer antigen 8
    Location1q43
    Gene typeprotein-coding
    SynonymsBBS16|CCCAP|CCCAP SLSN7|NPHP10|NY-CO-8|SLSN7|hCCCAP
    Quick linksEntrez ID:10806; HGNC:10671; MIM:613524; Ensembl:ENSG00000054282; HPRD:10215; Vega:OTTHUMG00000039996
    GO related
    GO term accessionGO term nameNumber of reference genesNumber of genesExpected numberRatio of enrichmentP-valueAdjusted P-Value
    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:0048646anatomical structure formation involved in morphogenesis15946219.833.134.32e-171.64e-15
    GO:0009653anatomical structure morphogenesis20557025.562.741.99e-167.08e-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:0005815microtubule organizing center486315.305.851.61e-152.87e-14
    GO:0015630microtubule cytoskeleton863379.413.935.76e-138.68e-12
    GO:0005813centrosome376224.105.361.49e-101.83e-09
    GO:0044430cytoskeletal part12873914.042.783.99e-093.91e-08
    GO:0005856cytoskeleton17904719.522.417.23e-096.16e-08
    GO:0044450microtubule organizing center part9491.038.788.63e-076.51e-06
    GO:0005814centriole5970.6410.883.47e-062.52e-05
    Pathway related
    TermSurceNumber of reference genesNumber of genesExpected numberRatio of enrichmentP-valueAdjusted P-value
    Loss of Nlp from mitotic centrosomesPathway commons6160.2721.873.47e-076.56e-06
    Golgi Cisternae Pericentriolar Stack ReorganizationPathway commons6260.2821.513.82e-076.56e-06
    Loss of proteins required for interphase microtubule organizationàfrom the centrosomePathway commons6160.2721.873.47e-076.56e-06
    Mitotic ProphasePathway commons6260.2821.513.82e-076.56e-06
    Centrosome maturationPathway commons7060.3119.057.91e-071.02e-05
    Recruitment of mitotic centrosome proteins and complexesPathway commons7060.3119.057.91e-071.02e-05
    G2/M TransitionPathway commons9660.4313.895.08e-065.23e-05
    Mitotic G2-G2/M phasesPathway commons9960.4513.476.07e-065.68e-05
    M PhasePathway commons15860.718.448.54e-050.0007
    DNA ReplicationPathway commons26171.175.960.00020.0015
    Cell Cycle, MitoticPathway commons31871.434.890.00060.0041
    Mitotic M-M/G1 phasesPathway commons24261.095.510.00080.0052
    PPI related
    IDNumber of reference genesNumber of genesExpected numberRatio of enrichmentP-valueAdjusted P-value
    Hsapiens_Module_2405560.5610.622.05e-050.0004
    OMIM related
    chromosomebeginenddisorder MIM numberdisorderphene mapping keygene/locus MIM numbercytogenetic loaction
    chr1243418306243664393613615Senior-Loken syndrome 736135241q43
    MGI related
    chromosomebeginendgene IDgene symbol of mouseMGIMPphenotype description
    chr124341830624366439310806Sdccag8MGI:1924066MP:0005367renal/urinary system phenotype
    chr124341830624366439310806Sdccag8MGI:1924066MP:0005371limbs/digits/tail phenotype
    chr124341830624366439310806Sdccag8MGI:1924066MP:0005381digestive/alimentary phenotype
    chr124341830624366439310806Sdccag8MGI:1924066MP:0005382craniofacial phenotype
    chr124341830624366439310806Sdccag8MGI:1924066MP:0010768mortality/aging
    Mutation spectrum

    If you cannot see the mutation spectrum below, please download and install the SVG plugin by clicking here.

    Gene-disease network

    If you cannot see the gene-disease network below, please download and install the SVG plugin by clicking here.


    Contact us if you are an author of a study regarding this gene and do not find your study in RetinoGenetics or find errors in the representation of your study details.