l(3)06911, d-spinophilin
Scaffolding protein - Neurexin/Neuroligin signalling - control of synaptic active zone number and functionality, a Protein-phosphatase 1 (PP1) targeting protein
Please see the JBrowse view of Dmel\Spn 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.
Tissue-specific extension of 3' UTRs observed during later stages (FBrf0218523, FBrf0219848); all variants may not be annotated
Gene model reviewed during 5.46
Low-frequency RNA-Seq exon junction(s) not annotated.
Annotated transcripts do not represent all possible combinations of alternative exons and/or alternative promoters.
Gene model reviewed during 5.55
Multiphase exon postulated: exon reading frame differs in alternative transcripts; overlap >20aa.
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\Spn 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: expression throughout the adult brain, higher in some regions
JBrowse - Visual display of RNA-Seq signals
View Dmel\Spn in JBrowse3-3
3-5.0
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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.
dsRNA made from templates generated with primers directed against this gene tested in RNAi screen for effects on Kc167 and S2R+ cell morphology.
Transcription unit spans the central region of the early-late puff at 62E.
Cloning and molecular analysis has identified the Spn transcription unit spanning at least 20 kb of genomic DNA from the central region of the 62E puff that is induced following the metamorphic pulse of ecdysone at the end of the third larval instar.
Source for merge of: E62 l(3)06911
Source for merge of: E62 CG16757
Source for merge of: Spn BcDNA:GM16129
Release 2 annotation CG16757 split into CG32295 and CG16757 (which corresponds to Spn) in release 3 of the genome annotation.
Source for merge of E62 CG16757 was sequence comparison ( date:001223 ).
Source for merge of Spn BcDNA:GM16129 was a shared cDNA ( date:030728 ).