Low-frequency RNA-Seq exon junction(s) not annotated.
Annotated transcripts do not represent all possible combinations of alternative exons and/or alternative promoters.
Gene model reviewed during 5.45
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\M7BP using the Feature Mapper tool.
GBrowse - Visual display of RNA-Seq signalsView Dmel\M7BP 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: M7BP CG43340
Source for merge of: CG30492 BcDNA:HL07907
One of the alternative 5' leading exons of CG30492 has been split out into its own separate annotation (CG43341) in release 5.36 of the genome annotation. The remainder of CG30492 has been merged with CG30494 to produce CG43340 in release 5.36 of the genome annotation.
Annotation CG2088 split into CG30492 and CG30494 ( BcDNA:GH02712 ) in release 3 of the genome annotation. In addition, release 3 annotation CG30492 contains sequences corresponding to release 2 annotations CG17984 and CG2080.
Comments: Source for merge of CG30492 BcDNA:HL07907 was a shared cDNA ( date:030728 ).
Shows particularly robust cycling of transcription in adult heads, as assessed by expression analysis using high density oligonucleotide arrays with probe generated during three 12-point time course experiments over the course of 6 days.