GC, Guanyl cyclase at 32E
Low-frequency RNA-Seq exon junction(s) not annotated.
Gene model reviewed during 5.52
Gene model reviewed during 5.40
Single-base exon is postulated.
Gene model reviewed during 5.57
4.5 (northern blot)
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\Gyc32E using the Feature Mapper tool.
Weak Gyc32E expression was observed in RNA from larvae and adult heads on northern blots. By in situ hybridization, transcripts are detected in ovaries in germarium regions 2 and 3. They disappear and then reappear at stage S10 in nurse cells. Gyc32E transcripts are uniform in very early embryos. Later they are confined to yolk and are not present in blastoderm cells. They reappear along the germ band of germ band elongated embryos.
GBrowse - Visual display of RNA-Seq signalsView Dmel\Gyc32E 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.
dsRNA made from templates generated with primers directed against this gene tested in RNAi screen for effects on Kc167 and S2R+ cell morphology.