Forkhead Box P2 Proteins (FOXP2)

FOXP2 encodes a member of the forkhead/winged-helix (FOX) family of transcription factors. Additionally we are shipping FOXP2 Antibodies (144) and and many more products for this protein.

list all proteins Gene Name GeneID UniProt
FOXP2 93986 O15409
FOXP2 114142 P58463
FOXP2 500037 P0CF24
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Top FOXP2 Proteins at

Showing 5 out of 6 products:

Catalog No. Origin Source Conjugate Images Quantity Supplier Delivery Price Details
Insect Cells Human His tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 1 mg Log in to see 60 Days
Insect Cells Mouse His tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 1 mg Log in to see 60 Days
HEK-293 Cells Human Myc-DYKDDDDK Tag Validation with Western Blot 20 μg Log in to see Available
Wheat germ Human GST tag 10 μg Log in to see 11 to 12 Days
Yeast Rat His tag   1 mg Log in to see 60 to 71 Days

FOXP2 Proteins by Origin and Source

Origin Expressed in Conjugate
Human , ,
, ,
Mouse (Murine)

Rat (Rattus)

More Proteins for Forkhead Box P2 (FOXP2) Interaction Partners

Human Forkhead Box P2 (FOXP2) interaction partners

  1. These findings suggest a novel miR (show MLXIP Proteins)-23a/FOXP2 link contributing to pancreatic ductal adenocarcinoma development and invasion.

  2. Data confirmed that miR196b could directly bind to 3'UTR of FOXP2 mRNA and repress its expression. miR196b and FOXP2 showed a negative correlation in HCC (show FAM126A Proteins) tissues. More importantly, upregulation of FOXP2 antagonized miR196bmediated migration and invasion in Hep3B cells. Furthermore, FOXP2 knockdown partially reversed the antimetastatic function of the miR196b inhibitor on HCCLM3 cells.

  3. SNPs in WNT2 (show WNT2 Proteins) and FOXP2 are associated with clinical symptom severity of autism spectrum disorders.

  4. we have identified a novel de novo missense variant in FOXP1 (show FOXP1 Proteins) that is identical to the most well-studied etiological variant in FOXP2. Functional characterization revealed clear similarities between these equivalent mutations in terms of their impact on protein function.

  5. FOXP2 anomaly is either directly or indirectly associated with atypical development of widespread subcortical networks early in life.

  6. Our findings suggest that the FOXP2 rs10447760 polymorphism may not contribute to the development of schizophrenia, but may contribute to the clinical symptoms of schizophrenia among Han Chinese

  7. FOXP2 frontal cortex expression abnormalities were identified in Frontotemporal Degeneration patients.

  8. Increased frequency of FOXP2 expression significantly correlated with FOXP1 (show FOXP1 Proteins)-positivity, and FOXP1 (show FOXP1 Proteins) co-immunoprecipitated FOXP2 from activated B-cell-diffuse large B-cell lymphoma (ABC (show ABCB6 Proteins)-DLBCL) cells.

  9. These findings suggest that miR (show MLXIP Proteins)-139 plays a suppressive role in the regulation of osteosarcoma cell proliferation and migration via directly targeting FOXP2.

  10. results provide evidence that FOXP2 SNPs influence aspects of human inner speech and fluency that are related to lateralized phenotypes, and suggest that the evolution of human language, as mediated by the adaptive evolution of FOXP2, involved features of inner speech

Mouse (Murine) Forkhead Box P2 (FOXP2) interaction partners

  1. findings also indicate that Foxp2 helps to regulate strength and length of hind limbs and maintenance of joint cartilage and intervertebral discs, which are all anatomical features that are susceptible to adaptations for bipedal locomotion.

  2. Foxp2 has a putative HuR (show ELAVL1 Proteins) binding sites in the 3' UTR. Phosphorylation sites on HuR (show ELAVL1 Proteins) act in post-transcriptional regulation of Foxp2.

  3. The expression levels of Foxp2 were high in the posterior region and low in the anterior region of the thalamic primordium.

  4. Here, the authors show that the telencephalic preoptic area is comprised of distinct progenitor pools complementarily marked by the transcription factors Dbx1 (show DBX1 Proteins) and Foxp2. As determined by molecular and electrophysiological criteria this embryonic parcellation predicts postnatal medial subnucleus of the amygdala inhibitory neuronal subtype identity.

  5. Eesults indicate a role of FoxP2 differential expression in cell morphology control of the vertebrate telencephalon.

  6. that Foxp2-Mef2C (show MEF2C Proteins) signaling is critical to corticostriatal circuit formation

  7. Sumoylation of forkhead box P2 in neonatal mouse cerebellum regulates Purkinje cell development and motor functions and vocal communication, demonstrating evidence for sumoylation in regulating mammalian behaviors.

  8. we demonstrated for the first time that Foxp1 (show FOXP1 Proteins) and Foxp2 are expressed during craniofacial development. Our data suggest that the Foxp genes may regulate development of the aboral and posterior regions of the jaw.

  9. Combined loss of all three Foxp1 (show FOXP1 Proteins)/2/4 family members in the developing anterior foregut endoderm leads to a loss of lung endoderm lineage commitment and subsequent development. Foxp1 (show FOXP1 Proteins)/2/4 deficient lungs express high levels of transcriptional regulators not normally expressed in developing lung. Ectopic expression of these transcriptional regulators is accompanied by decreased expression of lung restricted transcription.

  10. We show that Foxp1 (show FOXP1 Proteins) and the androgen receptor (show AR Proteins) are co-expressed in striatal medium spiny neurons and that brain-specific (show CALY Proteins) androgen receptor (show AR Proteins) KO (ArNesCre) mice exhibit reduced Foxp1 (show FOXP1 Proteins) expression in the striatum at E17.5 and P7.5 and an increased Foxp2 level in the cortex at P7.5. Thus, androgens may contribute to sex-specific differences in Foxp1 (show FOXP1 Proteins) and Foxp2 expression and ultrasonic vocalizations

Zebrafish Forkhead Box P2 (FOXP2) interaction partners

  1. Our findings suggest that foxP2 is not necessary for axon pathfinding during development.

  2. foxP2 likely has a more general conserved role in nervous system development; molecular cloning

  3. The developing optic tectum becomes the major area of FoxP2 expression. In the adult brain, the highest concentrations of the FoxP2 transcript can be observed in the optic tectum.

  4. Domain-specific regulation of foxP2 CNS expression by lef1 (show LEF1 Proteins).

FOXP2 Protein Profile

Protein Summary

This gene encodes a member of the forkhead/winged-helix (FOX) family of transcription factors. It is expressed in fetal and adult brain as well as in several other organs such as the lung and gut. The protein product contains a FOX DNA-binding domain and a large polyglutamine tract and is an evolutionarily conserved transcription factor, which may bind directly to approximately 300 to 400 gene promoters in the human genome to regulate the expression of a variety of genes. This gene is required for proper development of speech and language regions of the brain during embryogenesis, and may be involved in a variety of biological pathways and cascades that may ultimately influence language development. Mutations in this gene cause speech-language disorder 1 (SPCH1), also known as autosomal dominant speech and language disorder with orofacial dyspraxia. Multiple alternative transcripts encoding different isoforms have been identified in this gene.

Gene names and symbols associated with Forkhead Box P2 Proteins (FOXP2)

  • forkhead box P2 (FOXP2)
  • forkhead box P2 (Foxp2)
  • forkhead box P2 (foxp2)
  • forkhead box P2 (foxP2)
  • lmw-gs (Foxp2)
  • forkhead box transcription factor (foxp1c)
  • forkhead box P2 L homeolog (foxp2.L)
  • 2810043D05Rik protein
  • AI449000 protein
  • CAG-16 protein
  • cagh44 protein
  • D0Kist7 protein
  • foxP protein
  • Foxp2 protein
  • foxp2a protein
  • foxP2b protein
  • RGD1559697 protein
  • spch1 protein
  • tnrc10 protein
  • xlFoxP2 protein

Protein level used designations for Forkhead Box P2 Proteins (FOXP2)

CAG repeat protein 44 , forkhead box protein P2 , forkhead/winged-helix transcription factor , trinucleotide repeat containing 10 , trinucleotide repeat-containing gene 10 protein , forkhead box P2 , transcription factor FoxP2 , forkhead box P protein , lmw-gs , forkhead box transcription factor , xlFoxP2

93986 Homo sapiens
114142 Mus musculus
449627 Pan troglodytes
482413 Canis lupus familiaris
500037 Rattus norvegicus
505502 Bos taurus
555242 Danio rerio
613237 Macaca mulatta
751769 Taeniopygia guttata
769935 Gallus gallus
100101742 Xenopus (Silurana) tropicalis
100127352 Sus scrofa
100134847 Felis catus
100137387 Papio anubis
100144325 Oryctolagus cuniculus
100169841 Oryzias latipes
100303474 Saccoglossus kowalevskii
542882 Triticum aestivum
779033 Xenopus laevis
100439724 Pongo abelii
734154 Xenopus laevis
100990292 Pan paniscus
100717297 Cavia porcellus
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