l(1)BP1, l(1)9Fe, Q54, PRC1
Please see the JBrowse view of Dmel\feo for information on other features
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Gene model reviewed during 5.45
There is only one protein coding transcript and one polypeptide associated with this gene
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\feo using the Feature Mapper tool.
Comment: maternally deposited
GBrowse - Visual display of RNA-Seq signals
View Dmel\feo in GBrowse 21-33
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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: feo CG11207
Source for merge of: feo l(1)9Fe
dsRNA directed against this gene causes defects in cytokinesis when tested in an RNAi screen in S2 cells.
RNAi screen using dsRNA made from templates generated with primers directed against this gene causes a binucleation phenotype when assayed in Kc167 cells.
Mutant larval neuroblasts show severe defects in the assembly of both the central spindle and the contractile ring.
The gene is named "fascetto" (which means "thin bundle" in Italian) after the mutant phenotype; cells lacking feo function have thin central spindles during telophase.