secreted carbohydrate-binding protein involved in synapse assembly - modifier of signaling by the ligand Jelly belly and its receptor Alk
Please see the JBrowse view of Dmel\mtg 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
Gene model reviewed during 5.43
Gene model reviewed during 5.49
Gene model reviewed during 6.04
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\mtg 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).
mtg is mainly detected in embryos from stage 12 to 16. Lower levels are seen in later embryos and in larvae with a transient peak at L2. Expression again peaks on the third day after pupariation. Higher levels are seen in adult heads than bodies.
JBrowse - Visual display of RNA-Seq signals
View Dmel\mtg in JBrowsePlease 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.
mtg binds N-acetylglucosamine in a Ca[2+]-dependent manner.
Loss of mtg greatly reduces overall activity-dependent transmission.
mtg is required to form the specialised transsynaptic matrix that links the presynaptic active zone with the post-synaptic glutamate receptor domain in the synapse.
Mutants show dramatically impaired neurotransmission (98% reduced) exhibited at the embryonic neuromuscular junction. Ultrastructural analyses have revealed the loss of the highly structured extracellular matrix in the synaptic cleft of mutant neuromuscular junctions.
Source for merge of: mtg l(3)S084910b CG7549