Please see the JBrowse view of Dmel\fal for information on other features
To submit a correction to a gene model please use the Contact FlyBase form
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.
Gene model reviewed during 5.43
Gene model reviewed during 5.44
Gene model reviewed during 6.02
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\fal 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
JBrowse - Visual display of RNA-Seq signals
View Dmel\fal in JBrowse
3-45
3-42.5
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.
fal is required for correct morphogenetic movements during gastrulation.
Embryos derived from fal mutant females have severe gastrulation defects; they extend their germband, but since cells cannot move dorsally around the posterior pole, the entire ventral side of the embryo is thrown into folds.
Embryos derived from fal mutant females have severe gastrulation defects; numerous ectopic folds are formed on the ventral side of the embryo, because the germband elongates but cannot move around the posterior pole to the dorsal side.
Source for merge of: fal CG9670
Source for merge of fal CG9670 was sequence comparison ( date:010602 ).
