FGF20 wt Allele

Preferred Label : FGF20 wt Allele;

NCIt synonyms : Fibroblast Growth Factor 20 wt Allele; FGF-20; RHDA2;

NCIt definition : Human FGF20 wild-type allele is located within 8p22-p21.3 and is approximately 9 kb in length. This allele, which encodes fibroblast growth factor 20 protein, is involved in the survival of dopaminergic cells. Allelic variants are associated with Parkinson disease pathology.;

GenBank Accession Number : NM_019851;

Détails

Origin ID

C51425;

UMLS CUI

C1708013;

Automatic exact mappings (from CISMeF team)
- Fibroblast growth factor 20 [OMIM gene]
- Renal hypodysplasia/aplasia 2 [OMIM Phenotype]
- fibroblast growth factor 20 [ORDO Gene]
OMIM relation
- Fibroblast growth factor 20 [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
gene_found_in_organism
- Human [NCIt concept]
gene_has_physical_location
- 8: 16904045-16894705 [NCIt concept]
gene_in_chromosomal_location
- 8p22-p21.3 [NCIt concept]
gene_is_element_in_pathway
- Actin Cytoskeleton Regulation Pathway [NCIt concept]
- MAPK Signaling Pathway [NCIt concept]
- Melanoma Pathway [NCIt concept]
gene_plays_role_in_process
- Angiogenic Process [NCIt concept]
- Cell Differentiation Process [NCIt concept]
- Cell Proliferation Regulatory Process [NCIt concept]
- Cell Survival [NCIt concept]
- Heparin Binding [NCIt concept]
- Intercellular Communication Process [NCIt concept]
- Receptor Binding [NCIt concept]
- Receptor Signaling [NCIt concept]

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

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