Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\Frd using the Feature Mapper tool.
GBrowse - Visual display of RNA-Seq signalsView Dmel\Frd 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.
The Frd complementation group corresponds to one (or more) of the following annotated genes: CG42741, CG44252, CG44253, DCTN3-p24, CG9890, PPO3 (this mapping is based on the recessive lethality of the Frd1 chromosome). Frd may correspond to PPO3: FBrf0240659 shows that Frd1 mutants carry an intragenic deletion in PPO3.
M.G. Davis, 1961.