Gene model reviewed during 5.52
Gene model reviewed during 5.56
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\dy using the Feature Mapper tool.
GBrowse - Visual display of RNA-Seq signalsView Dmel\dy 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.
Source for identity of: dy CG9355
The 'Andante' mutant chromosome carries two independent EMS-induced mutations, one in dy (dyQ189stop) and one in CkIIβ (CkIIβAnd). The dyQ189stop mutation has no effect on rhythmicity, rather the CkIIβAnd allele is responsible for the circadian long-period phenotype of the mutant chromosome.
FBrf0054173 suggests that the 'Andante' mutant circadian rhythm phenotype maps to the dy locus. However, FBrf0151660 indicates that the 'Andante' mutant chromosome carries two separable lesions: a dy mutation that has no effect on rhythmicity and a mutation in CkIIβ which is responsible for the mutant circadian rhythm phenotype.
FBrf0054173 suggested that the 'Andante' mutation maps to the dy locus. See Jackson, 2002.7.26, personal communication to FlyBase for revision of that suggestion: the 'Andante' mutation maps to the CkIIβ locus - see CkIIβAnd. CkIIβAnd was found to be linked to an allele of dy, dyQ189stop, explaining the confusion.
Bridges, 1st Dec. 1916.