fd85E, forkhead domain 85E
forkhead domain transcription factor - a highly conserved transcription factor known for its importance in human speech and language production - reduced expression in Drosophila leads to decreased levels of courtship behavior, altered pulse-song structure, and sex-specific motor impairments in walking and flight
Please see the JBrowse view of Dmel\FoxP for information on other features
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Gene model reviewed during 5.49
Gene model reviewed during 5.44
Gene model reviewed during 5.41
Gene model reviewed during 5.39
Gene model reviewed during 5.56
Gene model reviewed during 6.05
None of the polypeptides share 100% sequence identity.
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\FoxP using the Feature Mapper tool.
Expression of FoxP protein overlaps with the expression of Scer\GAL4FoxP.1.5 except for cells in the posterior region of the ventral nerve cord that are not detected by the antibody against FoxP.
GBrowse - Visual display of RNA-Seq signals
View Dmel\FoxP in GBrowse 23-49
3-49
3-46.2
Please Note FlyBase no longer curates genomic clone accessions so this list may not be complete
Please Note This section lists cDNAs and ESTs that fall within the genomic extent of the gene model, which may include cDNAs and ESTs of genes within introns, or of overlapping genes. Please see GBrowse for alignment of the cDNAs and ESTs to the gene model.
For each fully sequenced cDNA the DGRC maintains various forms of the cDNA (e.g tagged or untagged) in several different host vectors for subsequent cloning and expression in Drosophila and Drosophila cell lines.
Source for identity of: fd85E CG16899
Source for identity of: FoxP fd85E
Source for merge of: fd85E CG32937
Annotations CG16899 and CG32937 merged as CG43067 in release 5.31 of the genome annotation.
One of 42 Drosophila genes identified as being most likely to reveal molecular and cellular mechanisms of nervous system development or plasticity relevant to human Mental Retardation disorders.
New annotation (CG32937) in release 3 of the genome annotation.