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    MBS3 Moebius syndrome 3 [ Homo sapiens (human) ]

    Gene ID: 22811, updated on 2-Oct-2019

    Summary

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    Gene symbol
    MBS3
    Gene description
    Moebius syndrome 3
    Primary source
    MIM:604185
    Gene type
    unknown
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    HCFP2

    Genomic context

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    Location:
    10q21.3-q22.1

    Bibliography

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    Related articles in PubMed

    1. A second gene for autosomal dominant Möbius syndrome is localized to chromosome 10q, in a Dutch family. Verzijl HT, et al. Am J Hum Genet, 1999 Sep. PMID 10441582, Free PMC Article
    2. Localization of a gene for Möbius syndrome to chromosome 3q by linkage analysis in a Dutch family. Kremer H, et al. Hum Mol Genet, 1996 Sep. PMID 8872479

    GeneRIFs: Gene References Into Functions

    Phenotypes

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    Moebius syndrome 3

    General gene information

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    Markers

    Other Names

    • hereditary congenital facial paresis 2

    Property

    • phenotype only

    Gene LinkOut

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