Please see the JBrowse view of Dmel\m-cup for information on other features
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Gene model reviewed during 5.48
None of the polypeptides share 100% sequence identity.
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\m-cup using the Feature Mapper tool.
Comment: maternally deposited
m-cup transcripts are detected at low levels in primary spermatocytes and are barely detected in early elongation spermatids. Robust signals are detected in more elongated spermatids at the distal ends. Transcripts localize in shallow cup-like shapes at the ends of spermatids bundles (called a cup pattern).
GBrowse - Visual display of RNA-Seq signals
View Dmel\m-cup in GBrowse 23-60
3-60
3-59.2
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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: m-cup CG11896
FlyBase curator comment: the insertion in the "e01527" Exelixis line (PBac{RB}CG12265e01527) was originally assigned to the CG11896 gene in FBrf0179797, resulting in the "CG11896e01527" (FBal0162515) allele. However, FBrf0184340 shows that the insertion is actually within CG12265.
The gene is named "mann-cup", based on the "cup"-like pattern of expression of the transcript in spermatid bundles; the mRNA localises in shallow cup-like shapes at the end of the spermatid bundles.