Quick Search:

  • Top 5 genes

    Top 5 diseases

    Data summary

    • Publications : 991
    • Phenotypes : 178
    • Genes : 207
    • Mutations : 4571
    • SNVs : 3402
    • InDels : 1169
    • Last Update : 26/10/2017

    Detailed information for ADAM9






    Basic information
    Official symbolADAM9
    Official full nameADAM metallopeptidase domain 9
    Location8p11.22
    Gene typeprotein-coding
    SynonymsCORD9|MCMP|MDC9|Mltng
    Quick linksEntrez ID:8754; HGNC:216; MIM:602713; Ensembl:ENSG00000168615; HPRD:04091; Vega:OTTHUMG00000159783
    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: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
    OMIM related
    chromosomebeginenddisorder MIM numberdisorderphene mapping keygene/locus MIM numbercytogenetic loaction
    chr83885350438963779612775Cone-rod dystrophy 936027138p11.22
    MGI related
    chromosomebeginendgene IDgene symbol of mouseMGIMPphenotype description
    chr838853504389637798754Adam9MGI:105376MP:0002873normal phenotype
    chr838853504389637798754Adam9MGI:105376MP:0005385cardiovascular system phenotype
    chr838853504389637798754Adam9MGI:105376MP:0005391vision/eye phenotype
    chr838853504389637798754Adam9MGI:105376MP: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.