U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

Links from OMIM

    • Showing Current items.

    MRT28 mental retardation, non-syndromic, autosomal recessive, 28 [ Homo sapiens (human) ]

    Gene ID: 100852396, updated on 31-Aug-2024

    Summary

    Go to the top of the page Help
    Official Symbol
    MRT28provided by HGNC
    Official Full Name
    mental retardation, non-syndromic, autosomal recessive, 28provided by HGNC
    Primary source
    MIM:614347
    Gene type
    unknown
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo

    Genomic context

    Go to the top of the page Help
    Location:
    6q26-q27

    Bibliography

    Go to the top of the pageHelp

    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

    Go to the top of the page Help

    Associated conditions

    Description Tests
    mental retardation, non-syndromic, autosomal recessive, 28
    OMIM: 614347GeneReviews: Not available

    General gene information

    Go to the top of the page Help

    Property

    • phenotype only

    Gene LinkOut

    The following LinkOut resources are supplied by external providers. These providers are responsible for maintaining the links.

    Molecular Biology Databases
    Research Materials