Gene model reviewed during 5.47
Annotated transcripts do not represent all possible combinations of alternative exons and/or alternative promoters.
Low-frequency RNA-Seq exon junction(s) not annotated.
Gene model reviewed during 5.55
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\dati using the Feature Mapper tool.
dati is specifically expressed in the CNS in embryos and is expressed in the brain and ventral nerve cord in larvae. It is not detected in other larval tissues (wing, eye, leg, and antennal discs). dati is expressed in a complex pattern that involves a few thousand neurons in the brain; about 2,400 central brian neurons (~6.6% of central brain neurons) express dati.
GBrowse - Visual display of RNA-Seq signalsView Dmel\dati 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.
FlyBase curator comment: The ‘l(4)102CDd’ locus was associated with 11 alleles through to FB2015_01. It was initially defined as a gene with two alleles, l(4)102CDd and l(4)102CDd, that failed to complement each other. FBrf0226419 shows that the only extant allele, l(4)102CDd, is really a deletion (‘Df(4)BH’) that deletes/disrupts 10 genes, including ‘dati’. It is not known whether the original l(4)102CDd allele, or other alleles in this lethal complementation group, are single lethals inside ‘Df(4)BH’ or also deletions, or whether these define one or more genes. As of FB2015_02, the ‘l(4)102CDd’ locus has been retained as a separate Gene Report, associated with 10 alleles (#1 and #3-11), while the l(4)102CDd allele is now an allele of ‘dati’ (owing to having a break-point in ‘dati’) that is associated with the deletion ‘Df(4)BH’.
Source for merge of CG2052 CG10204 was a shared cDNA ( date:010720 ).