FST wt Allele - CISMeF

Preferred Label : FST wt Allele;

NCIt synonyms : FS; Follistatin wt Allele;

NCIt definition : Human FST wild-type allele is located in the vicinity of 5q11.2 and is approximately 7 kb in length. This allele, which encodes follistatin protein, plays a role in inhibiting both follicle-stimulating hormone release and activin-mediated cell growth.;

NCIt note : Alternate splicing results in isoforms containing either 317 or 344 amino acids.;

GenBank Accession Number : NM_013409;

Details

Origin ID

C107132;

UMLS CUI

C3814419;

Automatic exact mappings (from CISMeF team)
- Feingold syndrome [ORDO Disease]
- Follistatin [ORDO Gene]
- Globoside alpha-1,3-n-acetylgalactosaminyltransferase [OMIM gene]
- snails [MeSH Descriptor]
- sulfur [MeSH Descriptor]
OMIM relation
- Follistatin [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]

Keyword's position in hierarchy(ies) :

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