U1, U1 snRNA
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\snRNA:U1:82Ec 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).
JBrowse - Visual display of RNA-Seq signals
View Dmel\snRNA:U1:82Ec in JBrowse3-[47.1]
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.
snRNA:U1:82Ec does not appear to be present in the D.melanogaster strain used for sequencing the genome; only one copy of a U1 snRNA gene (CR32862) has been detected at 82E in the sequenced strain, although 3 copies have previously been reported in clones derived from Oregon R flies - snRNA:U1:82Eb , snRNA:U1:82Ec and snRNA:U1:82Ea (FBrf0052749). The copy present in the sequenced strain appears to correspond to snRNA:U1:82Eb , while snRNA:U1:82Ec and snRNA:U1:82Ea appear to be missing from the sequenced strain (see FBrf0128209).
Sequences corresponding to snRNA:U1:82Ec have not been found on the Celera assembly on the date of analysis.
snRNA:U1:82Ec has been cloned and sequenced.
snRNA:U1:82Ec has been cloned and sequenced. snRNA:U1:82Ec is a pseudogene, it is deleted at the 5' end, missing the first 50 bases.