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    SHFM3 Split-hand/foot malformation 3 [ Homo sapiens (human) ]

    Gene ID: 100049542, updated on 31-Aug-2024

    Summary

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    Official Symbol
    SHFM3provided by HGNC
    Official Full Name
    Split-hand/foot malformation 3provided by HGNC
    Primary source
    MIM:246560
    Gene type
    unknown
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    SHSF3; DUP10q24; C10DUPq24

    Genomic context

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    Location:
    10q24

    Bibliography

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    Related articles in PubMed

    1. Maternal genes and facial clefts in offspring: a comprehensive search for genetic associations in two population-based cleft studies from Scandinavia. Jugessur A, et al. PLoS One, 2010 Jul 9. PMID 20634891, Free PMC Article

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?
    1. Observational study of gene-disease association. (HuGE Navigator)
      Title: Maternal genes and facial clefts in offspring: a comprehensive search for genetic associations in two population-based cleft studies from Scandinavia.
    Submit: New GeneRIF Correction

    Phenotypes

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    Associated conditions

    Description Tests
    Split-hand/foot malformation 3
    OMIM: 246560GeneReviews: Not available

    General gene information

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    Property

    • phenotype only

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