Please see the JBrowse view of Dmel\kat-60L1 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.
Low-frequency RNA-Seq exon junction(s) not annotated.
Gene model reviewed during 5.47
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\kat-60L1 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: Assay specific to short kat-60L1 transcripts (kat-60L1-RA, RD, RF and RH).
Comment: Transcripts encoding both kat-60L1 short (kat-60L1-RA, RD, RF and RH) and long transcripts (kat-60L1-RB, RC, RE, and RG) are expressed.
Both the short (kat-60L1-RA, kat-60L1-RD, kat-60L1-RF, and kat-60L1-RH) and long transcripts (kat-60L1-RB, kat-60L1-RC, kat-60L1-RE, and kat-60L1-RG) are expressed in adult testis. The short transcripts are also expressed in the third instar larval brains.
JBrowse - Visual display of RNA-Seq signals
View Dmel\kat-60L1 in JBrowse
3-47.5
3-44.1
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.
kat-60L1 is not required for the axonal projection of larval class IV da neurons, but it is required to establish their highly branched dendritic arbour and mediate their nocifensive functions.
kat-60L1 is not required for initial dendritic branch formation in the larva, but rather for arborization after 72 hours AEL during third-instar larval development.
kat-60L1 has a role in up-regulating the number, but not the rate, of growing microtubules in the dendrites of class IV neurons, thereby promoting branch stabilization of the dendritic arbor during third-instar larval development.
kat-60L1 is required for dendritic severing during dendrite pruning of ddaC neurons in the pupa.
dsRNA made from templates generated with primers directed against this gene tested in RNAi screen for effects on Kc167 and S2R+ cell morphology.
Source for identity of: kat-60L1 CG1193