lips, afadin, lip
Gene model reviewed during 5.47
Low-frequency RNA-Seq exon junction(s) not annotated.
Annotated transcripts do not represent all possible combinations of alternative exons and/or alternative promoters.
No evidence for 13aa QQQRYLGQSLPAE from SWP:Q24279 in the 18th exon of this gene.
Gene model reviewed during 6.03
8.2, 7.5, 7.0 (northern blot)
1893 (aa); 200 (kD observed)
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\cno using the Feature Mapper tool.
In wild type embryos, cno transcripts are expressed in dorsal-ventral oriented rows of cells in the posterior portion of each thoracic and abdominal segment. cno was shown to be induced by ubiquitous Ubx expression. cno expression in various homeotic mutant backgrounds was also described.
cno transcripts are most abundant in embryos, decrease in larvae, and increase again in pupae and adults. The relative abundance of the three transcript species varies with developmental stage. In early stage 5 embryos, a low uniform level of cno transcripts is seen. At the cellular blastoderm stage, expression is seen along the dorsal midline and in three ectodermal stripes in the central region of the embryo. During stages 7-10, expression is confined to the dorsal furrows and the posterior midgut rudiment. Ectodermal expression becomes evident in stage 10. In stage 13, focal stainings are detected near the attachment site of the midgut with the foregut and hindgut. In eye discs, cno is expressed ubiquitously with a higher concentration of transcripts in the lateral edge region.
GBrowse - Visual display of RNA-Seq signalsView Dmel\cno in GBrowse 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: cno CG2534
Annotations CG2534 and CG31537 merged as CG42312 in release 5.9 of the genome annotation.
"S(CycEJP)68S10" is unlikely to correspond to "cno"; mutations in the two loci complement each other.
Source for merge of cno anon-WO0172774.47 was sequence comparison ( date:051113 ).
Eleven further alleles (all EMS) discarded by Tubingen.
cno regulates linkage between adherens junctions and the actin cytoskeleton during morphogenesis.
RNAi generated by PCR using primers directed to this gene causes a cell growth and viability phenotype when assayed in Kc167 and S2R+ cells.
R and cno proteins act in the same molecular pathway during dorsal closure and the function of both proteins in dorsal closure depends on their ability to interact with each other. R acts upstream of cno in dorsal closure, but unlike cno, is not involved in the stimulation of JNK pathway activity.
dsRNA made from templates generated with primers directed against this gene tested in RNAi screen for effects on Kc167 and S2R+ cell morphology.
New annotation (CG31537) in release 3 of the genome annotation.
Mutants are isolated in an EMS mutagenesis screen to identify zygotic mutations affecting germ cell migration at discrete points during embryogenesis: mutants exhibit pattern defects (dorsal open).
The mechanism by which cno product controls cone cell formation in the developing compound eye is studied.