TnT, troponin T, TpnT, troponin-T, int
Please see the JBrowse view of Dmel\up for information on other features
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AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100. Some regions with low pLDDT may be unstructured in isolation.
Gene model reviewed during 5.55
Gene model reviewed during 5.42
Annotated transcripts do not represent all possible combinations of alternative exons and/or alternative promoters.
Low-frequency RNA-Seq exon junction(s) not annotated.
Annotated transcripts do not represent all supported alternative splices within 5' UTR.
Gene model reviewed during 5.51
Gene model reviewed during 5.56
1.9 (northern blot)
396, 387, 373 (aa)
Some glutamate residues are polyglycylated by TTLL3B. This modification occurs exclusively on glutamate residues and results in polyglycine chains on the gamma-carboxyl group.
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\up using the Feature Mapper tool.
The testis specificity index was calculated from modENCODE tissue expression data by Vedelek et al., 2018 to indicate the degree of testis enrichment compared to other tissues. Scores range from -2.52 (underrepresented) to 5.2 (very high testis bias).
Comment: maternally deposited
JBrowse - Visual display of RNA-Seq signals
View Dmel\up in JBrowseMapping based on up 'int' alleles.
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 JBrowse 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.
monoclonal
ChEST reveals this is a target of Mef2.
The genomic organisation of the up locus has been characterised.
Viability and fertility of up is good.
Fate mapping of up mutants suggests their primary site of action is in the presumptive thoracic musculature.
Electron microscope and electrophoresis studies indicate that these muscles lack internal structure in the Z-bands and Z-band proteins.
Wings held upright and mutants unable to jump or fly when homo- or hemizygous. The indirect flight muscles of the thorax are abnormal, with many mitochondria in the muscle fiber envelopes but with defective myofibrils; which contain half the normal amount of Z-band proteins.
Source for merge of: up BcDNA:LD08591
Source for merge of up BcDNA:LD08591 was a shared cDNA ( date:030728 ).