Low-frequency RNA-Seq exon junction(s) not annotated.
Annotated transcripts do not represent all supported alternative splices within 5' UTR.
Gene model reviewed during 5.52
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\fusl using the Feature Mapper tool.
fusl protein is detected in the retina, lamina and medulla in young adults, where it is found at the plasma membrane and is enriched at presynaptic termini. Several different assays on larval neuromuscular junctions reveal that it is membrane-associated and restricted to the extreme periphery of synaptic boutons.
GBrowse - Visual display of RNA-Seq signalsView Dmel\fusl 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: fusl CG14021
fusl regulates assembly of the presynaptic active zone Ca[2+] channel domains required for efficient coupling of the Ca[2+] influx and synaptic vesicle exocytosis during neurotransmission.