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    EJM2 epilepsy, juvenile myoclonic 2 [ Homo sapiens (human) ]

    Gene ID: 50715, updated on 31-Aug-2024

    Summary

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    Official Symbol
    EJM2provided by HGNC
    Official Full Name
    epilepsy, juvenile myoclonic 2provided by HGNC
    Primary source
    MIM:604827
    Gene type
    unknown
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    JME; EIG7

    Genomic context

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    Location:
    15q14

    Bibliography

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    Related articles in PubMed

    1. Genetic mapping of a major susceptibility locus for juvenile myoclonic epilepsy on chromosome 15q. Elmslie FV, et al. Hum Mol Genet, 1997 Aug. PMID 9259280

    GeneRIFs: Gene References Into Functions

    Phenotypes

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    Associated conditions

    Description Tests
    epilepsy, juvenile myoclonic 2
    OMIM: 604827GeneReviews: Not available

    General gene information

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    Markers

    Other Names

    • myoclonic epilepsy, juvenile, 2

    Property

    • phenotype only

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