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    CORD1 cone rod dystrophy 1 (autosomal dominant) [ Homo sapiens (human) ]

    Gene ID: 1319, updated on 2-Oct-2019

    Summary

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    Gene symbol
    CORD1
    Gene description
    cone rod dystrophy 1 (autosomal dominant)
    Primary source
    MIM:600624
    Gene type
    unknown
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    CORD; CRD1

    Genomic context

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    Location:
    18q21.1-q21.3

    Bibliography

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    Related articles in PubMed

    1. Deletion mapping of a retinal cone-rod dystrophy: assignment to 18q211. Warburg M, et al. Am J Med Genet, 1991 Jun 1. PMID 1867279

    GeneRIFs: Gene References Into Functions

    Phenotypes

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    cone rod dystrophy 1 (autosomal dominant)

    General gene information

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    Property

    • phenotype only

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