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    DEL10Q26 Chromosome 10q deletion syndrome [ Homo sapiens (human) ]

    Gene ID: 780911, updated on 16-Aug-2019

    Summary

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    Gene symbol
    DEL10Q26
    Gene description
    Chromosome 10q deletion syndrome
    Primary source
    MIM:609625
    Gene type
    unknown
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    TQDS; C10q26DEL

    Genomic context

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    Location:
    10q26

    Bibliography

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    Related articles in PubMed

    1. The chromosome 10q26 susceptibility locus in age-related macular degeneration. Stanton CM, et al. Adv Exp Med Biol, 2012. PMID 22183354

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?
    1. Chromosome 10q26 susceptibility locus may be involved in age related macular degeneration.
      Title: The chromosome 10q26 susceptibility locus in age-related macular degeneration.
    Submit: New GeneRIF Correction

    Phenotypes

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    Chromosome 10q deletion syndrome

    General gene information

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    Property

    • phenotype only

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