FST (follistatin)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 10468 |
| Gene name | Follistatin |
| Gene symbol | FST |
| Synonyms (NCBI Gene) |
FS
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| Chromosome | 5 |
| Chromosome location | 5q11.2 |
| Summary | Follistatin is a single-chain gonadal protein that specifically inhibits follicle-stimulating hormone release. The single FST gene encodes two isoforms, FST317 and FST344 containing 317 and 344 amino acids respectively, resulting from alternative splicin |
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miRNA
miRNA information provided by mirtarbase database.
50
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Transcription factors
Transcription factors information provided by TRRUST V2 database.
5
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Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
31
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Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
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Protein
Protein information from UniProt database.
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UniProt ID
Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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P19883 | |||||||||||||||||||||||||
| Protein name | Follistatin (FS) (Activin-binding protein) | |||||||||||||||||||||||||
| Protein function | Multifunctional regulatory protein whose primary function is to antagonize members of the transforming growth factor beta (TGF-beta) superfamily including activin, myostatin, GDF11 or bone morphogenetic proteins (BMPs) (PubMed:11279126, PubMed:1 | |||||||||||||||||||||||||
| PDB | 2B0U , 2P6A , 3HH2 , 5JHW | |||||||||||||||||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Isoform 1 is the predominant isoform in serum but is undetectable in follicular fluid. In the embryo, strong expression is seen in the palatal epithelia, including the medial edge epithelial and midline epithelial seam of the palatal s | |||||||||||||||||||||||||
| Sequence |
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| Sequence length | 344 | |||||||||||||||||||||||||
| Interactions | View interactions | |||||||||||||||||||||||||
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Pathways
Pathway information has different metabolic/signaling pathways associated with genes.
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Associated diseases
Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
1
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