Gene model reviewed during 5.52
Low-frequency RNA-Seq exon junction(s) not annotated.
Annotated transcripts do not represent all supported alternative splices within 5' UTR.
Annotated transcripts do not represent all possible combinations of alternative exons and/or alternative promoters.
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\PhKγ using the Feature Mapper tool.
GBrowse - Visual display of RNA-Seq signalsView Dmel\PhKγ 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: PhKγ CG1830
When dsRNA constructs are made and transiently transfected into S2 cells in RNAi experiments, an increase in cytokinetic index, central spindle defects, and lagging chromatids are seen.
Transcriptionally downregulated after 2h of insulin stimulation in Kc167 cells. Contains fkh response elements (FHREs) in the genomic upstream or intronic sequences.
PhKγ is required in early embryonic processes, such as gastrulation and mesoderm formation. Defects in these processes are only seen when the maternal and zygotic components are eliminated.
The existence of this gene was predicted on the basis of a match of the STS sequence read from the T7 promoter of European Cosmid 194B3 whose translation shows 53% identity (67% similarity) with a human phosphorylase B kinase γ catalytic chain protein sequence (SwissProt P15735).