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    MRT24 mental retardation, non-syndromic, autosomal recessive, 24 [ Homo sapiens (human) ]

    Gene ID: 100852402, updated on 31-Aug-2024

    Summary

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    Official Symbol
    MRT24provided by HGNC
    Official Full Name
    mental retardation, non-syndromic, autosomal recessive, 24provided by HGNC
    Primary source
    MIM:614345
    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:
    6p12

    Bibliography

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    Related articles in PubMed

    1. Homozygosity mapping in 64 Syrian consanguineous families with non-specific intellectual disability reveals 11 novel loci and high heterogeneity. Abou Jamra R, et al. Eur J Hum Genet, 2011 Nov. PMID 21629298, Free PMC Article

    GeneRIFs: Gene References Into Functions

    Phenotypes

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    Associated conditions

    Description Tests
    mental retardation, non-syndromic, autosomal recessive, 24
    OMIM: 614345GeneReviews: Not available

    General gene information

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    Property

    • phenotype only

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