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    DEL11P13 Chromosome 11p13 deletion syndrome, distal [ Homo sapiens (human) ]

    Gene ID: 107648861, updated on 31-Aug-2024

    Summary

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    Official Symbol
    DEL11P13provided by HGNC
    Official Full Name
    Chromosome 11p13 deletion syndrome, distalprovided by HGNC
    Primary source
    MIM:616902
    Gene type
    unknown
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    C11DELp13

    Genomic context

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    Location:
    11p13

    Bibliography

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    GeneRIFs: Gene References Into Functions

    Phenotypes

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    Associated conditions

    Description Tests
    Chromosome 11p13 deletion syndrome, distal
    OMIM: 616902GeneReviews: Not available

    General gene information

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    Property

    • phenotype only

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    Molecular Biology Databases