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    DEL17Q12 Chromosome 17q12 deletion syndrome [ Homo sapiens (human) ]

    Gene ID: 100884130, updated on 31-Aug-2024

    Summary

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    Official Symbol
    DEL17Q12provided by HGNC
    Official Full Name
    Chromosome 17q12 deletion syndromeprovided by HGNC
    Primary source
    MIM:614527
    Gene type
    unknown
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    C17DELq12

    Genomic context

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    Location:
    17q12

    Bibliography

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    Related articles in PubMed

    1. Duplications of 17q12 can cause familial fever-related epilepsy syndromes. Hardies K, et al. Neurology, 2013 Oct 15. PMID 24049133

    GeneRIFs: Gene References Into Functions

    Phenotypes

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    Associated conditions

    Description Tests
    Chromosome 17q12 deletion syndrome
    OMIM: 614527GeneReviews: Not available

    General gene information

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    Property

    • phenotype only

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