Please see the JBrowse view of Dmel\Sf3b3 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 5.48
Gene model reviewed during 5.44
Gene model reviewed during 5.55
None of the polypeptides share 100% sequence identity.
Identified in the spliceosome A complex; remains associated with the spliceosome throughout the splicing process (By similarity). Component of the spliceosome B complex (By similarity). Identified in the spliceosome C complex (By similarity). Identified in the spliceosome E complex (By similarity). Component of the U11/U12 snRNPs that are part of the U12-type spliceosome (By similarity). Component of splicing factor SF3B complex (PubMed:18981222). Identified in the SAGA transcription regulatory histone acetylation (HAT) complex; the interaction is RNA-independent (PubMed:27185460).
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\Sf3b3 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
Comment: reported as muscle system primordium
Comment: reported as muscle system primordium
JBrowse - Visual display of RNA-Seq signals
View Dmel\Sf3b3 in JBrowse





3-0.5
3-0.7
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.
Nonsense-mediated mRNA decay (NMD) down-regulates a distinct splice isoform(s) of this gene.
RNAi screen using dsRNA made from templates generated with primers directed against this gene results in a long metaphase spindle with misaligned chromosomes when assayed in S2 cells. This phenotype can be observed when the screen is performed with or without Cdc27 dsRNA.
Area matching Drosophila EST AA567184.
The "l(3)0083500835" allele fails to complement alleles of the "l(3)61Db-S" and "l(3)61Dc" loci to varying extents. This suggests that the "l(3)61Db-S" and "l(3)61Dc" loci may be physically close to each other so that the single P-element insertion that causes "l(3)0083500835" (P{PZ}l(3)0083500835) may impair the function of both genes. From the position of the P{PZ}l(3)0083500835 insertion, it is likely that "l(3)61Db-S" and "l(3)61Dc" correspond to "CG13900" and "CG13886", although a one-to-one assignment cannot be established.
Source for identity of: Sf3b3 CG13900