koj, kojak, lincRNA.286
Low-frequency RNA-Seq exon junction(s) not annotated.
Gene model reviewed during 5.45
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\sha using the Feature Mapper tool.
GBrowse - Visual display of RNA-Seq signalsView Dmel\sha in GBrowse 2
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.
sv mutants results in a lack of sensory bristles, but has no phenotype in trichomes while sha mutants has no phenotype in bristles but results in a dramatic loss of denticles and trichomes. The sv and sha mutant phenotypes are thus distinct.
Mutant alleles are useful as markers in clonal analysis.
The gene is named "kojak" for the bald phenotype seen in some cells.