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    MRT10 mental retardation, non-syndromic, autosomal recessive, 10 [ Homo sapiens (human) ]

    Gene ID: 100101425, updated on 31-Aug-2024

    Summary

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    Official Symbol
    MRT10provided by HGNC
    Official Full Name
    mental retardation, non-syndromic, autosomal recessive, 10provided by HGNC
    Primary source
    MIM:611096
    Gene type
    unknown
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    MRT20

    Genomic context

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    Location:
    16p12-q12

    Bibliography

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    Related articles in PubMed

    1. Homozygosity mapping in consanguineous families reveals extreme heterogeneity of non-syndromic autosomal recessive mental retardation and identifies 8 novel gene loci. Najmabadi H, et al. Hum Genet, 2007 Mar. PMID 17120046

    GeneRIFs: Gene References Into Functions

    Phenotypes

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    Associated conditions

    Description Tests
    mental retardation, non-syndromic, autosomal recessive, 10
    OMIM: 611096GeneReviews: Not available

    General gene information

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    Property

    • phenotype only

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