val, 38B.5
scaffolding protein - the substrate recognition platform for the arginine methyltransferase Capsuleen - the primary substrates of Capsuleen and Valois are the spliceosomal Sm proteins - required for accumulation of high levels of Oskar protein, for posterior localization of Oskar in later stages of oogenesis and for posterior localization of the Vasa protein during pole plasm assembly
Please see the JBrowse view of Dmel\vls 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.
Gene model reviewed during 5.44
Gene model reviewed during 5.52
There is only one protein coding transcript and one polypeptide associated with this gene
Interacts with csul and tud.
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\vls 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).
Comment: maternally deposited
Comment: anlage in statu nascendi
Comment: anlage in statu nascendi
Comment: anlage in statu nascendi
Comment: anlage in statu nascendi
Comment: reported as procephalic ectoderm anlage in statu nascendi
Comment: reported as procephalic ectoderm anlage in statu nascendi
Comment: reported as procephalic ectoderm anlage in statu nascendi
Comment: reported as procephalic ectoderm anlage
Comment: reported as procephalic ectoderm anlage
Comment: reported as procephalic ectoderm anlage
Comment: reported as procephalic ectoderm anlage
Comment: reported as procephalic ectoderm primordium
Comment: reported as procephalic ectoderm primordium
Comment: reported as procephalic ectoderm primordium
Comment: reported as procephalic ectoderm primordium
Comment: reported as procephalic ectoderm primordium
Comment: reported as procephalic ectoderm primordium
JBrowse - Visual display of RNA-Seq signals
View Dmel\vls in JBrowse





2-54
2-53.9
2-[54]
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.
Distribution of tud protein in mutant embryos has been studied.
vls is not required for the nurse cell synthesis of the posterior signal.
Mutations in maternal posterior class gene vls do not interact with RpII140wimp.
Mature follicles are immunologically stained for asymmetric distribution of ecdysteroid-related antigen. During late oogenesis localisation of the antigen changes dramatically suggesting the antigen plays a role in early embryogenesis and, perhaps, in pattern formation.
In vls mutant females the vas protein is localized to the posterior pole of oocytes, this localization is lost following egg activation. There is a low level of vas distributed throughout the embryo.
vls plays a role in polar granule formation.
Mutations in vls result in a maternal effect phenotype with defects during cellularisation of the blastoderm and a "grandchildless knirps-like" phenotype.
Mutations in vls cause failure of germ cell formation and deletions in the abdominal segments of the embryo.
Source for merge of: vls CG10728
"lok" may be allelic to "vls".