loe, loechrig, AMPKγ, SNF4A, SNF4
Low-frequency RNA-Seq exon junction(s) not annotated.
Annotated transcripts do not represent all possible combinations of alternative exons and/or alternative promoters.
Annotated transcripts do not represent all supported alternative splices within 5' UTR.
Gene model reviewed during 5.46
The group(s) of polypeptides indicated below share identical sequence to each other.
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\SNF4Aγ using the Feature Mapper tool.
GBrowse - Visual display of RNA-Seq signalsView Dmel\SNF4Aγ 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.
Annotations CG17299 and CG5806 merged as CG17299 in release 3 of the genome annotation.
Southern analysis suggests that SNF4 is present as two copies in the genome that are relatively divergent.
Source for merge of SNF4Aγ anon-WO0118547.338 anon-WO0118547.575 anon-WO0257455.21 was sequence comparison ( date:051113 ).
Nonsense-mediated mRNA decay (NMD) down-regulates a distinct splice isoform(s) of this gene.
Area matching Drosophila EST AA539974.
Mutants show age-dependent neurodegeneration.
Gene was called 'lochrig' by the authors which is the German word for 'full of holes'.