FGF12 wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human FGF12 wild-type allele is located within 3q28-q29 and is approximately 329 kb in length. This allele, which encodes fibroblast growth factor 12 protein, is involved in the development and function of the nervous system. Mutation of the gene is associated with early infantile epileptic encephalopathy.

**Synonyms:** - EIEE47 - FGF-12 - FGF12B - FHF-1 - FHF1 - Fibroblast Growth Factor 12 wt Allele - Fibroblast Growth Factor 12B Gene - Fibroblast Growth Factor FGF-12b Gene