Low-frequency RNA-Seq exon junction(s) not annotated.
Gene model reviewed during 5.46
A pair of annexin repeats may form one binding site for calcium and phospholipid.
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\AnxB11 using the Feature Mapper tool.
GBrowse - Visual display of RNA-Seq signalsView Dmel\AnxB11 in GBrowse 2
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 merge of: Anxb11 BcDNA:GH16395
FlyBase curator comment: Renamed from 'Anxb11' to 'AnxB11' in order to make the nomenclature of D. melanogaster Annexins consistent with each other and with the standard Annexin nomenclature.
Source for identity of Anxb11 CG9968 was sequence comparison ( date:000407 ).
Source for merge of Anxb11 BcDNA:GH16395 was TrEMBL update ( date:020807 ).
dsRNA made from templates generated with primers directed against this gene tested in RNAi screen for effects on Kc167 and S2R+ cell morphology.
RNAi screen using dsRNA made from templates generated with primers directed against this gene causes a phenotype when assayed in S2R+ cells: cells become round and detached. Kc167 cells are unaffected.