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    OPA4 optic atrophy 4 (autosomal dominant) [ Homo sapiens (human) ]

    Gene ID: 58156, updated on 31-Aug-2024

    Summary

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    Official Symbol
    OPA4provided by HGNC
    Official Full Name
    optic atrophy 4 (autosomal dominant)provided by HGNC
    Primary source
    MIM:605293
    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:
    18q12.2

    Bibliography

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    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?
    1. Second locus is linked to 18q12.2-q12.3 (OPA4
      Title: [Genetic basis of hereditary optic atrophies].
    Submit: New GeneRIF Correction

    Phenotypes

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    Associated conditions

    Description Tests
    optic atrophy 4 (autosomal dominant)
    OMIM: 605293GeneReviews: Not available

    General gene information

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    Markers

    Property

    • phenotype only

    Gene LinkOut

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