Aliases for FOS Gene
- Fos Proto-Oncogene, AP-1 Transcription Factor Subunit 2 3 5
- FBJ Murine Osteosarcoma Viral Oncogene Homolog 2 3
- G0/G1 Switch Regulatory Protein 7 3 4
- FBJ Murine Osteosarcoma Viral (V-Fos) Oncogene Homolog (Oncogene FOS) 3
- Fos Proto-Oncogene, AP-1 Trancription Factor Subunit 3
- V-Fos FBJ Murine Osteosarcoma Viral Oncogene Homolog 2
- Cellular Oncogene C-Fos 3
- Cellular Oncogene Fos 4
External Ids for FOS Gene
Previous GeneCards Identifiers for FOS Gene
The Fos gene family consists of 4 members: FOS, FOSB, FOSL1, and FOSL2. These genes encode leucine zipper proteins that can dimerize with proteins of the JUN family, thereby forming the transcription factor complex AP-1. As such, the FOS proteins have been implicated as regulators of cell proliferation, differentiation, and transformation. In some cases, expression of the FOS gene has also been associated with apoptotic cell death. [provided by RefSeq, Jul 2008]
GeneCards Summary for FOS Gene
FOS (Fos Proto-Oncogene, AP-1 Transcription Factor Subunit) is a Protein Coding gene. Diseases associated with FOS include Acute Pericementitis and Pertussis. Among its related pathways are ERK Signaling and Gene Expression. Gene Ontology (GO) annotations related to this gene include DNA binding transcription factor activity and transcription factor binding. An important paralog of this gene is FOSL2.
UniProtKB/Swiss-Prot for FOS Gene
Nuclear phosphoprotein which forms a tight but non-covalently linked complex with the JUN/AP-1 transcription factor. In the heterodimer, FOS and JUN/AP-1 basic regions each seems to interact with symmetrical DNA half sites. On TGF-beta activation, forms a multimeric SMAD3/SMAD4/JUN/FOS complex at the AP1/SMAD-binding site to regulate TGF-beta-mediated signaling. Has a critical function in regulating the development of cells destined to form and maintain the skeleton. It is thought to have an important role in signal transduction, cell proliferation and differentiation. In growing cells, activates phospholipid synthesis, possibly by activating CDS1 and PI4K2A. This activity requires Tyr-dephosphorylation and association with the endoplasmic reticulum.