Dlic2, l(1)G0065, l(1)G0190, dandelion clock
Please see the JBrowse view of Dmel\Dlic for information on other features
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AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100. Some regions with low pLDDT may be unstructured in isolation.
Low-frequency RNA-Seq exon junction(s) not annotated.
Annotated transcripts do not represent all supported alternative splices within 5' UTR.
Gene model reviewed during 5.51
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\Dlic using the Feature Mapper tool.
The testis specificity index was calculated from modENCODE tissue expression data by Vedelek et al., 2018 to indicate the degree of testis enrichment compared to other tissues. Scores range from -2.52 (underrepresented) to 5.2 (very high testis bias).
Dlic localizes to the presumptive oocyte early in oogenesis and by mid-oogenesis, it localizes to the posterior pole of the oocyte.
JBrowse - Visual display of RNA-Seq signals
View Dmel\Dlic in JBrowse
1-33
1-34.8
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 JBrowse 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.
polyclonal
monoclonal
Dlic is required for polarised dendritic transport and uniform microtubule orientation in axons.
RNAi screen using dsRNA made from templates generated with primers directed against this gene causes spindle pole detachment when assayed in S2 cells. This phenotype can be observed when the screen is performed with or without Cdc27 dsRNA.
Mutants in dlic form smaller dendritic receptor fields. Terminals of major branches keep extending without further branching and some of pre-existing side branches retract; in contrast, the proximal region becomes bushy over time.
dsRNA made from templates generated with primers directed against this gene tested in RNAi screen for effects on Kc167 and S2R+ cell morphology.
Source for merge of: Dlic2 l(1)G0065 l(1)G0190
Source for identity of: Dlic2 CG1938
The name "dandelion clock" refers to the "bushy" dendritic arbor phenotype of homozygous "Dlic[1]" mutant neurons.