CG 6811
Please see the JBrowse view of Dmel\RhoGAP68F 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 5.43
Low-frequency RNA-Seq exon junction(s) not annotated.
Annotated transcripts do not represent all possible combinations of alternative exons and/or alternative promoters.
Gene model reviewed during 5.46
Gene model reviewed during 6.45
The group(s) of polypeptides indicated below share identical sequence to each other.
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\RhoGAP68F 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
Expression in stage P3 pupal leg discs is restricted to presumptive tarsal joints.
JBrowse - Visual display of RNA-Seq signals
View Dmel\RhoGAP68F in JBrowse
3-38
3-30.9
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
RhoGAP68F localises preferentially to Rab4 endosomes and forms a complex with the Rab4 protein. RhoGAP68F inhibits the direct return of Rab4 endosomes containing Fas3 and shg back to the cell surface. The upregulation of RhoGAP68F during prepupal development is thus predicted to result in decreased transport of key cell adhesion proteins to the cell surface, decreasing the strength of cell-cell contacts and facilitating epithelial remodeling during morphogenesis.
dsRNA made from templates generated with primers directed against this gene tested in RNAi screen for effects on Kc167 and S2R+ cell morphology.