FOXP2
Gene Ontology | |
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Molecular function | • DNA binding • chromatin binding • double-stranded DNA binding • sequence-specific DNA binding transcription factor activity • RNA polymerase II distal enhancer sequence-specific DNA binding transcription factor activity • transcription factor binding • zinc ion binding • DNA binding, bending • protein homodimerization activity • sequence-specific DNA binding • protein heterodimerization activity |
Cellular component | • nucleus • transcription factor complex • nucleolus • cytoplasm |
Biological process | • positive regulation of mesenchymal cell proliferation • pattern specification process • skeletal muscle tissue development • embryo development • post-embryonic development • cerebellum development • caudate nucleus development • putamen development • cerebral cortex development • growth • vocal learning • camera-type eye development • negative regulation of transcription, DNA-dependent • lung alveolus development • smooth muscle tissue development • regulation of sequence-specific DNA binding transcription factor activity • righting reflex • positive regulation of epithelial cell proliferation involved in lung morphogenesis |
Sources: Amigo / QuickGO |
113.73 – 114.33 Mb
14.9 – 15.44 Mb
Forkhead box protein P2 also known as FOXP2 is a protein that in humans is encoded by the FOXP2 gene, located on human chromosome 7 (7q31, at the SPCH1 locus). FOXP2 orthologs have also been identified in all mammals for which complete genome data are available. The FOXP2 protein contains a forkhead-box DNA-binding domain, making it a member of the FOX group of transcription factors, involved in regulation of gene expression. In addition to this characteristic forkhead-box domain, the protein contains a polyglutamine tract, a zinc finger and a leucine zipper.
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