Mutation in sequenced strain: deletion; 31-bp deletion within coding region.
Possible pseudogene, as described in FBrf0211681.
Gene model reviewed during 5.48
May be a polymorphic pseudogene (intact in some individuals or strains, disrupted by mutation in others).
There is only one protein coding transcript and one polypeptide associated with this gene
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\Ir10a using the Feature Mapper tool.
GBrowse - Visual display of RNA-Seq signalsView Dmel\Ir10a 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.
Source for identity of: Ir10a CG34143
Source for merge of: CG12624 CG12623
The Ir10a gene, one of 44 "divergent" ionotropic receptor genes in D. melanogaster, may have been derived from an ancestral ionotropic receptor gene by retroposition, and in some cases, subsequent gene duplication.
Annotations CG12624 and CG12623 merged as CG34143 in release 5.1 of the genome annotation.