negative regulation of transcription by RNA polymerase II
regulation of reactive oxygen species metabolic process
transcription, DNA-templated
regulation of neural precursor cell proliferation
cellular response to dexamethasone stimulus
cellular response to DNA damage stimulus
neuronal stem cell population maintenance
autophagy
positive regulation of transcription, DNA-templated
response to insulin
blood vessel development
cellular response to cold
response to fluoride
regulation of cell population proliferation
cellular response to insulin stimulus
positive regulation of apoptotic process
negative regulation of stress-activated MAPK cascade
cellular response to oxidative stress
enamel mineralization
cellular response to nitric oxide
positive regulation of gluconeogenesis
temperature homeostasis
negative regulation of transcription, DNA-templated
fat cell differentiation
negative regulation of canonical Wnt signaling pathway
endocrine pancreas development
protein acetylation
positive regulation of transcription by RNA polymerase II
cellular response to hydrogen peroxide
apoptotic process
anatomical structure morphogenesis
cell differentiation
negative regulation of cardiac muscle hypertrophy in response to stress
cytokine-mediated signaling pathway
energy homeostasis
Sources:Amigo / QuickGO
Orthologs
Species
Human
Mouse
Entrez
2308
56458
Ensembl
ENSG00000150907
ENSMUSG00000044167
UniProt
Q12778
Q9R1E0
RefSeq (mRNA)
NM_002015
NM_019739
RefSeq (protein)
NP_002006
NP_062713
Location (UCSC)
Chr 13: 40.56 – 40.67 Mb
Chr 3: 52.18 – 52.26 Mb
PubMed search
[3]
[4]
Wikidata
View/Edit Human
View/Edit Mouse
Forkhead box protein O1 (FOXO1), also known as forkhead in rhabdomyosarcoma (FKHR), is a protein that in humans is encoded by the FOXO1 gene.[5] FOXO1 is a transcription factor that plays important roles in regulation of gluconeogenesis and glycogenolysis by insulin signaling, and is also central to the decision for a preadipocyte to commit to adipogenesis.[6] It is primarily regulated through phosphorylation on multiple residues; its transcriptional activity is dependent on its phosphorylation state.[7][8]
^ abcGRCh38: Ensembl release 89: ENSG00000150907 – Ensembl, May 2017
^ abcGRCm38: Ensembl release 89: ENSMUSG00000044167 – Ensembl, May 2017
^"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^"Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^Galili N, Davis RJ, Fredericks WJ, Mukhopadhyay S, Rauscher FJ, Emanuel BS, Rovera G, Barr FG (November 1993). "Fusion of a fork head domain gene to PAX3 in the solid tumour alveolar rhabdomyosarcoma". Nature Genetics. 5 (3): 230–5. doi:10.1038/ng1193-230. PMID 8275086. S2CID 12374322.
^Nakae J, Kitamura T, Kitamura Y, Biggs WH, Arden KC, Accili D (January 2003). "The forkhead transcription factor Foxo1 regulates adipocyte differentiation". Developmental Cell. 4 (1): 119–29. doi:10.1016/S1534-5807(02)00401-X. PMID 12530968.
^Rena G, Guo S, Cichy SC, Unterman TG, Cohen P (June 1999). "Phosphorylation of the transcription factor forkhead family member FKHR by protein kinase B". The Journal of Biological Chemistry. 274 (24): 17179–83. doi:10.1074/jbc.274.24.17179. PMID 10358075.
^Guo S, Rena G, Cichy S, He X, Cohen P, Unterman T (June 1999). "Phosphorylation of serine 256 by protein kinase B disrupts transactivation by FKHR and mediates effects of insulin on insulin-like growth factor-binding protein-1 promoter activity through a conserved insulin response sequence". The Journal of Biological Chemistry. 274 (24): 17184–92. doi:10.1074/jbc.274.24.17184. PMID 10358076.
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