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    DEL17Q11.2 chromosome 17q11.2 deletion syndrome [ Homo sapiens (human) ]

    Gene ID: 100852404, updated on 12-Mar-2017
    Gene symbol
    DEL17Q11.2
    Gene description
    chromosome 17q11.2 deletion syndrome
    Primary source
    MIM:613675
    Gene type
    unknown
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    C17DELq11.2

    GeneRIFs: Gene References Into FunctionsWhat's a GeneRIF?

    Other Names

    • NF1 microdeletion syndrome
    • neurofibromatosis 1 microdeletion syndrome

    Property

    • phenotype only
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