MyoV, myosin V, shorty, DmV, MyoV43CD
Gene model reviewed during 5.48
Low-frequency RNA-Seq exon junction(s) not annotated.
Alternative translation stop created by use of multiphasic reading frames within coding region.
None of the polypeptides share 100% sequence identity.
1792 (aa); 207 (kD predicted)
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\didum using the Feature Mapper tool.
didum transcripts are detected in embryos and adults on northern blots. Maternally derived transcripts are uniformly distributed in embryos up to stage 6. Later in embryogenesis, high levels of didum transcript are observed in the ectodermal tissue of the hindgut.
didum transcripts are detected in adult ovaries and testes and at low levels in embryos by northern blots. They are detected by in situ hybridization in ovaries. They are localized to the oocyte from germarial stage 2 and are confined to the anterior margin of the oocyte during the middle stages of oogenesis (6-8). In late vitellogenic stages (9-11), there is strong staining in nurse cells and a loss of anterior localization in the oocyte.
GBrowse - Visual display of RNA-Seq signalsView Dmel\didum in GBrowse 2
Maps to 2R.
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: didum CG2146
"l(2)43Cc" may correspond to "didum"; there is a band shift in the didum genomic region associated with the "l(2)43Cc4" mutation which is not a polymorphism, although it maps several kilobases 5' of the cloned genomic didum sequence.
Source for merge of didum NEST:bs14c05 was sequence comparison ( date:031022 ).
One of 42 Drosophila genes identified as being most likely to reveal molecular and cellular mechanisms of nervous system development or plasticity relevant to human Mental Retardation disorders.
dsRNA made from templates generated with primers directed against this gene tested in RNAi screen for effects on Kc167 and S2R+ cell morphology.
dsRNA made from templates generated with primers directed against this gene is tested in an RNAi screen for effects on actin-based lamella formation.
Area matching Drosophila myosin V gene (inverted), Acc. No. AF003826.