SCUBA

FOXO1 — Forkhead box O1

FOXO1 belongs to a gene co-expression module in 5 of 28 SCUBA cell types. Each module groups genes that rise and fall together in that cell type; the genes it shares a module with are its closest co-expression partners there.

FOXO1's module in each cell type

Cell typeModuleShares the module with
CD4⁺ T cellsImmune Regulation
Immune regulation
ADAT2, AFTPH, C2CD4B, CDKL2, CPEB4, DDHD1, FAM53B, FAS +10 moreView in SCUBA
EndothelialInflammatory ECM Remodeling
ECM remodeling
CNTNAP3B, CYB5RL, IL7, ITSN1, KIF3C, KRT8, LRCH2, MMP16 +6 moreView in SCUBA
Gamma-delta T cellsTCR Threshold Regulation
TCR Signaling
AGO2, ATP8A1, AUTS2, CMIP, CNOT6L, CSNK1D, GSPT1, MAP3K8 +8 more
MacrophagesTranscriptional Kinase Regulation
Housekeeping
BNC2, CABLES1, CACNB4, CDK8, ENOX2, FAF1, INPP4B, JMY +17 moreView in SCUBA
Mucosal-associated invariant T cellT cell Quiescence
T cell maturation
AGO2, AUTS2, BCL6, BRD1, CSNK1D, DHCR7, GABPB1, GAL3ST2 +13 more

About the gene

SynonymsFKH1, FKHR, FOXO1A
Chromosome13: 40555667-40666641
Predicted locationIntracellular
Essential geneNo
Protein classCancer-related genes, Disease related genes, Human disease related genes, Predicted intracellular proteins, Transcription factors
Molecular functionActivator, DNA-binding
Biological processApoptosis, Autophagy, Differentiation, Transcription, Transcription regulation

Function

Transcription factor that is the main target of insulin signaling and regulates metabolic homeostasis in response to oxidative stress. Binds to the insulin response element (IRE) with consensus sequence 5'-TT[G/A]TTTTG-3' and the related Daf-16 family binding element (DBE) with consensus sequence 5'-TT[G/A]TTTAC-3'. Activity suppressed by insulin. Main regulator of redox balance and osteoblast numbers and controls bone mass (By similarity). Orchestrates the endocrine function of the skeleton in regulating glucose metabolism (By similarity). Also acts as a key regulator of chondrogenic commitment of skeletal progenitor cells in response to lipid availability: when lipids levels are low, translocates to the nucleus and promotes expression of SOX9, which induces chondrogenic commitment and suppresses fatty acid oxidation (By similarity). Acts synergistically with ATF4 to suppress osteocalcin/BGLAP activity, increasing glucose levels and triggering glucose intolerance and insulin insensitivity (By similarity). Also suppresses the transcriptional activity of RUNX2, an upstream activator of osteocalcin/BGLAP (By similarity). Acts as an inhibitor of glucose sensing in pancreatic beta cells by acting as a transcription repressor and suppressing expression of PDX1 (By similarity). In hepatocytes, promotes gluconeogenesis by acting together with PPARGC1A and CEBPA to activate the expression of genes such as IGFBP1, G6PC1 and PCK1 (By similarity). Also promotes gluconeogenesis by directly promoting expression of PPARGC1A and G6PC1. Important regulator of cell death acting downstream of CDK1, PKB/AKT1 and STK4/MST1. Promotes neural cell death. Mediates insulin action on adipose tissue (By similarity). Regulates the expression of adipogenic genes such as PPARG during preadipocyte differentiation and, adipocyte size and adipose tissue-specific gene expression in response to excessive calorie intake (By similarity). Regulates the transcriptional activity of GADD45A and repair of nitric oxide-damaged DNA in beta-cells (By similarity). Required for the autophagic cell death induction in response to starvation or oxidative stress in a transcription-independent manner. Mediates the function of MLIP in cardiomyocytes hypertrophy and cardiac remodeling (By similarity). Positive regulator of apoptosis in cardiac smooth muscle cells as a result of its transcriptional activation of pro-apoptotic genes. Regulates endothelial cell (EC) viability and apoptosis in a PPIA/CYPA- dependent manner via transcription of CCL2 and BCL2L11 which are involved in EC chemotaxis and apoptosis.

Human Protein Atlas · Open Targets · UniProt

Gene annotation from the Human Protein Atlas and UniProt; see sources & licences.