FGF14 wt Allele

Preferred Label : FGF14 wt Allele;

NCIt synonyms : FHF4; SCA27; BA397O8.2; Fibroblast Growth Factor 14 wt Allele; FHF-4; FGF-14;

NCIt definition : Human FGF14 wild-type allele is located in the vicinity of 13q33.1 and is approximately 692 kb in length. This allele, which encodes fibroblast growth factor 14 protein, plays a role in nervous system development. Mutation of the gene is associated with spinocerebellar ataxia 27.;

NCI Metathesaurus CUI : CL545847;

GenBank Accession Number : NM_001321931;

Détails

Origin ID

C147992;

UMLS CUI

C4553226;

Automatic exact mappings (from CISMeF team)
- Fibroblast growth factor 14 [OMIM gene]
- Spinocerebellar ataxia type 27 [ORDO Disease]
- fibroblast growth factor 14 [ORDO Gene]
- fibroblast growth factor 14 [MeSH Supplementary Concept]
- spinocerebellar ataxia 27 [MeSH Supplementary Concept]
OMIM relation
- Fibroblast growth factor 14 [OMIM gene]
See also inter- (CISMeF)
- Spinocerebellar ataxia 27 [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]
- Intercellular Communication Process [NCIt concept]
- Nervous System Development [NCIt concept]
- Receptor Binding [NCIt concept]
- Receptor Signaling [NCIt concept]

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

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