TRPN1, TRPN, jf24, l(2)jf24
Gene model reviewed during 6.03
Gene model reviewed during 5.41
Low-frequency RNA-Seq exon junction(s) not annotated.
Gene model reviewed during 5.52
Annotated transcripts do not represent all possible combinations of alternative exons and/or alternative promoters.
Gene model reviewed during 6.05
6.151 (longest cDNA)
None of the polypeptides share 100% sequence identity.
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\nompC using the Feature Mapper tool.
Expression of nompC is seen as a dot at the base of each mechanosensory bristle of the abdominal cuticle. Ultrastructurally, it is localized at the apical tip of the dendritic cilia in tactile bristles. Expression of nompC in the scolopidia of the Johnston's organ is concentrated in the distal tip of the cilia in each Johnston's organ scolopidium, specifically in the region enclosed by the cap.
GBrowse - Visual display of RNA-Seq signalsView Dmel\nompC 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.
nompC encodes an ion channel that is essential for mechanosensory transduction.
Bristle recordings of mutant flies show almost complete loss of mechanoreceptor potential (MRP). Mutations cause adult inviability due to severe uncoordination.