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    GINGF3 gingival fibromatosis, hereditary, 3 [ Homo sapiens (human) ]

    Gene ID: 780916, updated on 31-Aug-2024

    Summary

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    Official Symbol
    GINGF3provided by HGNC
    Official Full Name
    gingival fibromatosis, hereditary, 3provided by HGNC
    Primary source
    MIM:609955
    Gene type
    unknown
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    GGF3; HGF3

    Genomic context

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    Location:
    2p23.3-p22.3

    Bibliography

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    Related articles in PubMed

    1. Refinement of the GINGF3 locus for hereditary gingival fibromatosis. Pampel M, et al. Eur J Pediatr, 2010 Mar. PMID 19633868, Free PMC Article
    2. A novel locus for autosomal dominant hereditary gingival fibromatosis, GINGF3, maps to chromosome 2p22.3-p23.3. Ye X, et al. Clin Genet, 2005 Sep. PMID 16098013

    GeneRIFs: Gene References Into Functions

    Phenotypes

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    Associated conditions

    Description Tests
    gingival fibromatosis, hereditary, 3
    OMIM: 609955GeneReviews: Not available

    General gene information

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    Property

    • phenotype only

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