ESTS:199A6T , ESTS:143G11T , Ub, Ubiquitin
Please see the JBrowse view of Dmel\CG11700 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.
Partial duplication of Ubi-p53 (CG32744); result of 4-kb tandem duplication. Appears to be functional (FBrf0218166).
Gene model reviewed during 5.46
Low-frequency RNA-Seq exon junction(s) not annotated.
Gene model reviewed during 5.50
There is only one protein coding transcript and one polypeptide associated with this gene
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\CG11700 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).
JBrowse - Visual display of RNA-Seq signals
View Dmel\CG11700 in JBrowse1-16
1-16.3
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.
Annotation CR11700 renamed CG11700 in release 5.46 of the genome annotation.
Ubi-p5E and CG11700 were derived from a single event of segmental tandem duplication. Both encode putative Ubiquitins. Ubi-p5E is conserved, ubiquitously expressed, and likely retains the function of the ancestral gene, whereas CG11700 has accumulated many nonsynonymous substitutions, has a male-specific pattern, and has likely undergone neofunctionalization.
Annotation CG11700 renamed CR11700 in release 5.2 of the genome annotation.
RNAi generated by PCR using primers directed to this gene causes a cell growth and viability phenotype when assayed in Kc167 and S2R+ cells.
RNAi screen using dsRNA made from templates generated with primers directed against this gene causes a cell growth and viability phenotype when assayed in Kc167 and S2R+ cells.
Source for identity of: CR11700 CG11700
Source for identity of: CG11700 CR11700