small GTPase - intermediate-term memory generated after single cycle conditioning is divided into anesthesia-sensitive memory and anesthesia-resistant memory - expressed in the mushroom body - physically interacts with cacaphony
Please see the JBrowse view of Dmel\Rgk1 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.
Gene model reviewed during 5.47
None of the polypeptides share 100% sequence identity.
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\Rgk1 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).
Rgk1 protein is specifically expressed in Kenyon cells. Expression is stronger in the lobes than in the calyx or Kenyon cell bodies. Antibody specific to Rgk1-PB shows strong expression in the alpha/beta and gamma neurons and weak expression in the alpha'/beta' neurons. In the gamma lobes, Rgk1 protein is observed in puncta that colocalize with the brp signal and is thought to be associated with presynapses of Kenyon cells.
JBrowse - Visual display of RNA-Seq signals
View Dmel\Rgk1 in JBrowse2-89
2-94.3
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.
RNAi generated by PCR using primers directed to this gene causes a cell growth and viability phenotype when assayed in Kc167 and S2R+ cells.
dsRNA made from templates generated with primers directed against this gene tested in RNAi screen for effects on Kc167 and S2R+ cell morphology.
New annotation (CG30127) in release 3 of the genome annotation.
Source for merge of: Rgk1 CG30127
Annotations CG9811 and CG30127 merged as CG44011 in release 5.47 of the genome annotation. Merge supported by RNA-seq junction data.
Source for identity of: Rgk1 CG9811