dGlcAT-P
Please see the JBrowse view of Dmel\GlcAT-P for information on other features
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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 5.45
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\GlcAT-P using the Feature Mapper tool.
Comment: maternally deposited
Comment: anlage in statu nascendi
Comment: GlcAT-P isoforms RB, RC, and RE
GlcAT-P isoforms RB, RC, and RE are detected throughout development and in various tissues (body wall, larval CNS, fat body) by qRT-PCR with the lowest levels in late embryonic stages and in larval fat body and the highest levels in adult female bodies.
GBrowse - Visual display of RNA-Seq signals
View Dmel\GlcAT-P in GBrowse 23-35
3-28.7
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.
polyclonal
Source for identity of: GlcAT-P CG6207
Source for identity of GlcAT-P CG6207 was sequence comparison ( date:030311 ).
GlcAT-P is required in hemocytes for aspects of glial cell biology which in turn affect the elongation of peripheral nerves during larval development.