Cenp-E, DmCmeta, l(2)04431
Please see the GBrowse view of Dmel\cmet or the JBrowse view of Dmel\cmet for information on other features
To submit a correction to a gene model please use the Contact FlyBase form
Gene model reviewed during 5.45
Annotated transcripts do not represent all possible combinations of alternative exons and/or alternative promoters.
Low-frequency RNA-Seq exon junction(s) not annotated.
7.524 (longest cDNA)
None of the polypeptides share 100% sequence identity.
2244 (aa); 250, 180 (kD observed); 257 (kD predicted)
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\cmet using the Feature Mapper tool.
cmet associates with centromeric regions of chromosomes, probably kinetochores.
GBrowse - Visual display of RNA-Seq signals
View Dmel\cmet in GBrowse 22-44
2-44
2-37.9
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.
Source for merge of: cmet CG6392
Source for merge of: cmet l(2)04431
Source for merge of cmet CG6392 was sequence comparison ( date:000725 ).
RNAi screen using dsRNA made from templates generated with primers directed against this gene results in chromosome misalignment on the metaphase spindle when assayed in S2 cells. This phenotype can be observed when the screen is performed with or without Cdc27 dsRNA.
dsRNA made from templates generated with primers directed against this gene tested in RNAi screen for effects on Kc167 and S2R+ cell morphology.
RNAi screen using dsRNA made from templates generated with primers directed against this gene causes a phenotype when assayed in S2R+ cells: cell morphology is aberrant, indicative of a failure in cell cycle/mitosis progression. This phenotype is not seen in Kc167 cells.
cmet is required for the maintenance of chromosomes at the metaphase plate.
The autosomal "FLP-DFS" technique (using the P{ovoD1-18} P{FRT(whs)} P{hsFLP} chromosomes) has been used to identify the specific maternal effect phenotype for the zygotic lethal mutation. cmet gene expression during oogenesis is not critical to embryonic development, but the gene function may be essential for fertilisation and/or completion of meiosis.
