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    CMD1H cardiomyopathy, dilated 1H (autosomal dominant) [ Homo sapiens (human) ]

    Gene ID: 23459, updated on 2-Oct-2019

    Summary

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    Gene symbol
    CMD1H
    Gene description
    cardiomyopathy, dilated 1H (autosomal dominant)
    Primary source
    MIM:604288
    Gene type
    unknown
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo

    Genomic context

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    Location:
    2q14-q22

    Bibliography

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    Related articles in PubMed

    1. Investigation of a family with autosomal dominant dilated cardiomyopathy defines a novel locus on chromosome 2q14-q22. Jung M, et al. Am J Hum Genet, 1999 Oct. PMID 10486326, Free PMC Article

    GeneRIFs: Gene References Into Functions

    Phenotypes

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    cardiomyopathy, dilated 1H (autosomal dominant)

    General gene information

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    Markers

    Property

    • phenotype only

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