Interacts with PRC1 complex member polycomb protein Pc; the interaction targets Pc for ubiquitin-independent proteasomal degradation. Does not interact with PRC1 members Ph, Psc or Sce so does not appear to be a member of the PRC1 complex. Interacts with 26S proteasome regulatory subunit Rpn10.
The ubiquitin-like domain is required for Pc degradation.
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\stx using the Feature Mapper tool.
GBrowse - Visual display of RNA-Seq signalsView Dmel\stx in GBrowse 2
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 GBrowse 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.
Source for identity of: stx CG32676
Source for merge of: CG9725 CG9732
Annotations CG9725, CG9732 merged as CG32676 in release 3 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.