FGF22 wt Allele

Preferred Label : FGF22 wt Allele;

NCIt synonyms : UNQ2500/PRO5800; Fibroblast Growth Factor 22 wt Allele;

NCIt definition : Human FGF22 wild-type allele is located in the vicinity of 19p13.3 and is approximately 4 kb in length. This allele, which encodes fibroblast growth factor 22 protein, plays a role in both glucose homeostasis and lipid metabolism.;

GenBank Accession Number : NM_020637;

Details

Origin ID

C120955;

UMLS CUI

C4055024;

OMIM relation
- Fibroblast growth factor 22 [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_in_chromosomal_location
- 19p13.3 [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]
- Carbohydrate Metabolic Process [NCIt concept]
- Cell Differentiation Process [NCIt concept]
- Cell Proliferation Regulatory Process [NCIt concept]
- Heparin Binding [NCIt concept]
- Intercellular Communication Process [NCIt concept]
- Lipid Metabolic Process [NCIt concept]
- Receptor Binding [NCIt concept]
- Receptor Signaling [NCIt concept]

Keyword's position in hierarchy(ies) :

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