FGF13 wt Allele

Preferred Label : FGF13 wt Allele;

NCIt synonyms : FGF2; FHF2; Fibroblast Growth Factor 13 wt Allele; RP6-27P15.3; Fibroblast Growth Factor Homologous Factor 2 Gene; FHF-2; FGF-13;

NCIt definition : Human FGF13 wild-type allele is located in the vicinity of Xq26.3 and is approximately 591 kb in length. This allele, which encodes fibroblast growth factor 13 protein, is involved in microtubule polymerization, neural development and neuronal migration. Deletion of the region of the X chromosome where the gene is located is associated with Borjeson-Forssman-Lehmann syndrome.;

GenBank Accession Number : BC034340;

Details

Origin ID

C118514;

UMLS CUI

C3890231;

Automatic exact mappings (from CISMeF team)
- Fibroblast growth factor 13 [OMIM gene]
- Fibroblast growth factor 2 [OMIM gene]
- fibroblast growth factor 13 [MeSH Supplementary Concept]
- fibroblast growth factor 13 [ORDO Gene]
- fibroblast growth factor 17 [ORDO Gene]
- fibroblast growth factor 2 [MeSH Descriptor]
OMIM relation
- Fibroblast growth factor 13 [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
concept_is_in_subset
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
gene_found_in_organism
- Human [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]
- Heparin Binding [NCIt concept]
- Intercellular Communication Process [NCIt concept]
- Negative Regulation of Microtubule Depolymerization [NCIt concept]
- Nervous System Development [NCIt concept]
- Receptor Binding [NCIt concept]
- Receptor Signaling [NCIt concept]
- Tubulin Binding [NCIt concept]

Keyword's position in hierarchy(ies) :

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