Please see the JBrowse view of Dmel\bnk for information on other features
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AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100. Some regions with low pLDDT may be unstructured in isolation.
Gene model reviewed during 5.47
Gene model reviewed during 5.53
1.2 (northern blot)
There is only one protein coding transcript and one polypeptide associated with this gene
303 (aa); 33.5 (kD)
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\bnk using the Feature Mapper tool.
The testis specificity index was calculated from modENCODE tissue expression data by Vedelek et al., 2018 to indicate the degree of testis enrichment compared to other tissues. Scores range from -2.52 (underrepresented) to 5.2 (very high testis bias).
Comment: 2-4 hr AEL
bnk transcripts are first detected during nuclear division cycle 11. They reach a strong peak with the onset of cycle 14 and then levels drop precipitously.
bnk protein is localized to the cellularization front, where it colocalizes with myosin, during cellularization of the embryo.
JBrowse - Visual display of RNA-Seq signals
View Dmel\bnk in JBrowse3-102
3-99.1
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 JBrowse 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.
bnk acts as a crosslinker/stabiliser of actin filaments.
dsRNA made from templates generated with primers directed against this gene tested in RNAi screen for effects on Kc167 and S2R+ cell morphology.
Area matching Drosophila Bottleneck gene (inverted), Acc. No. U01035.
Phenotypic analysis is based on deficiency chromosomes.
The expression pattern and mutant phenotype of bnk suggests a direct role in regulating the dynamic restructuring of the actin-based cytoskeleton of cellularizing embryos.
Mutant embryos lacking the cellularization locus, bnk, exhibit a variety of defects including premature 'closing off' of the actin/myosin contractile ring.
Source for identity of: bnk CG1480