FGF12 wt Allele

Preferred Label : FGF12 wt Allele;

NCIt synonyms : FHF1; Fibroblast Growth Factor 12B Gene; Fibroblast Growth Factor FGF-12b Gene; FGF12B; Fibroblast Growth Factor 12 wt Allele; EIEE47; FHF-1; FGF-12;

NCIt 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.;

NCI Metathesaurus CUI : CL545848;

GenBank Accession Number : U66197;

Détails

Origin ID

C147993;

UMLS CUI

C4553635;

Automatic exact mappings (from CISMeF team)
- Fibroblast growth factor 12 [OMIM gene]
- fibroblast growth factor 12 [ORDO Gene]
OMIM relation
- Fibroblast growth factor 12 [OMIM gene]
See also inter- (CISMeF)
- Developmental and epileptic encephalopathy 47 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
gene_found_in_organism
- Human [NCIt concept]
gene_plays_role_in_process
- Angiogenic Process [NCIt concept]
- Cell Differentiation Process [NCIt concept]
- Cell Proliferation Regulatory Process [NCIt concept]
- Heparin Binding [NCIt concept]
- Nervous System Development [NCIt concept]
- Neuronal Transmission [NCIt concept]
- Receptor Binding [NCIt concept]
- Receptor Signaling [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

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