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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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