FOS
Protein c-Fos
Also known as: AP-1, c-fos, FOS_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P01100
- Gene
- FOS
- Ensembl
- ENSG00000170345
- Chromosome
- 14
- Canonical length
- 380 aa
- Protein class
- Cancer-related genes, Predicted intracellular proteins, Transcription factors
- Subcellular location
- Nucleoplasm
OverviewNCBI 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]
Canonical amino-acid sequenceUniProt
380 residues, UniProt reviewed canonical sequence.
>P01100|FOS
1 MMFSGFNADY EASSSRCSSA SPAGDSLSYY HSPADSFSSM GSPVNAQDFC TDLAVSSANF
61 IPTVTAISTS PDLQWLVQPA LVSSVAPSQT RAPHPFGVPA PSAGAYSRAG VVKTMTGGRA
121 QSIGRRGKVE QLSPEEEEKR RIRRERNKMA AAKCRNRRRE LTDTLQAETD QLEDEKSALQ
181 TEIANLLKEK EKLEFILAAH RPACKIPDDL GFPEEMSVAS LDLTGGLPEV ATPESEEAFT
241 LPLLNDPEPK PSVEPVKSIS SMELKTEPFD DFLFPASSRP SGSETARSVP DMDLSGSFYA
301 ADWEPLHSGS LGMGPMATEL EPLCTPVVTC TPSCTAYTSS FVFTYPEADS FPSCAAAHRK
361 GSSSNEPSSD SLSSPTLLALLocalizationUniProt · AlphaFold · HPA
Whether an antibody against FOS can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.68
- Highest tissue expression
- 2,146 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 2,146 nTPM
- skin: 1,567 nTPM
- esophagus: 1,178 nTPM
- ovary: 1,091 nTPM
- gallbladder: 1,088 nTPM
- fallopian tube: 1,084 nTPM
Single-cell type
- neutrophils: 6,882 nCPM
- decidual stromal cells: 6,299 nCPM
- endometrial luminal cells: 6,203 nCPM
- ovarian stromal cells: 5,794 nCPM
- breast secretory cells: 4,280 nCPM
- smooth muscle cells: 4,047 nCPM
Immune cell
- neutrophil: 507 nTPM
- eosinophil: 90 nTPM
- classical monocyte: 81 nTPM
- myeloid DC: 70 nTPM
- basophil: 38 nTPM
- total PBMC: 28 nTPM
Brain region
- hypothalamus: 367 nTPM
- cerebellum: 333 nTPM
- medulla oblongata: 264 nTPM
- white matter: 205 nTPM
- choroid plexus: 195 nTPM
- cerebral cortex: 190 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about FOS.
Disease | GeneticClinVar
1 pathogenic / likely-pathogenic of 51 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.65
- gnomAD pLI
- 0.26
- gnomAD missense Z
- 1.08
- DepMap mean gene effect
- -0.07
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cellular response to calcium ion
- cellular response to epidermal growth factor stimulus
- cellular response to hypoxia
- cellular response to parathyroid hormone stimulus
- cellular response to phorbol 13-acetate 12-myristate
- cellular response to reactive oxygen species
- cellular response to tumor necrosis factor
- cellular response to zinc ion starvation
- cerebral cortex development
- conditioned taste aversion
- female pregnancy
- inflammatory response
- integrated stress response signaling
- mononuclear cell differentiation
- myoblast proliferation
- neural retina development
- neuron differentiation
- osteoclast differentiation
- positive regulation of DNA-templated transcription
- positive regulation of miRNA transcription
- positive regulation of osteoclast differentiation
- positive regulation of transcription by RNA polymerase II
- regulation of transcription by RNA polymerase II
- response to activity
- response to cAMP
- response to corticosterone
- response to ethanol
- response to forskolin
- response to gravity
- response to immobilization stress
- response to insulin
- response to light stimulus
- response to lipopolysaccharide
- response to muscle stretch
- response to progesterone
- response to toxic substance
- response to xenobiotic stimulus
- skeletal muscle cell differentiation
- skeletal muscle cell proliferation
- SMAD protein signal transduction
- transcription by RNA polymerase II
- transforming growth factor beta receptor signaling pathway
- cellular response to prolactin
- medium-term memory
Molecular functions
- DNA-binding transcription activator activity, RNA polymerase II-specific
- DNA-binding transcription factor activity
- DNA-binding transcription factor activity, RNA polymerase II-specific
- identical protein binding
- promoter-specific chromatin binding
- protein-containing complex binding
- R-SMAD binding
- RNA polymerase II cis-regulatory region sequence-specific DNA binding
- RNA polymerase II core promoter sequence-specific DNA binding
- RNA polymerase II-specific DNA-binding transcription factor binding
- sequence-specific double-stranded DNA binding
- transcription cis-regulatory region binding
- transcription coregulator binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of FOS in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads FOS as an antibody target. Whether an autoantibody or antibody against FOS could matter depends on whether native FOS is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
FOS is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label FOS as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
Loading the interactive Seroatlas protein explorer...