l(3)07013, 91F, 91F gene, B9.3
Please see the GBrowse view of Dmel\cdi or the JBrowse view of Dmel\cdi for information on other features
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Gene model reviewed during 5.54
Tissue-specific extension of 3' UTRs observed during later stages (FBrf0218523, FBrf0219848); all variants may not be annotated
Gene model reviewed during 6.02
None of the polypeptides share 100% sequence identity.
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\cdi using the Feature Mapper tool.
Expression pattern inferred from unspecified enhancer trap line.
cdi transcripts are detected at all stages of embryogenesis as well as in larvae, pupae, and adults on northern blots. Only the shortest isoform is observed in early embryos and may be maternally transmitted. In situ hybridization shows nervous system expression specifically in the midline in both neurons and glia. Expression is also observed in the foregut, hindgut, and proventriculus.
cdi protein is found throughout the eye-antennal disc. The localization is cytoplasmic and more prominent in the apical domains of the eye disc epithelium.
GBrowse - Visual display of RNA-Seq signals
View Dmel\cdi in GBrowse 23-65
3-65
3-65.2
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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 merge of: cdi l(3)07013
Source for merge of cdi l(3)07013 was a shared cDNA ( date:030206 ).
dsRNA made from templates generated with primers directed against this gene tested in RNAi screen for effects on Kc167 and S2R+ cell morphology.
Identified as a target gene regulated by the bithorax complex.
The autosomal "FLP-DFS" technique (using the P{ovoD1-18} P{FRT(whs)} P{hsFLP} chromosomes) has been used to identify the specific maternal effect phenotype for the zygotic lethal mutation.
cdi encodes a novel protein kinase.
