Allele Dmel\Dscam3.31.8
| General Information | |||
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| Symbol | Dmel\Dscam3.31.8 | Species | D. melanogaster |
| Name | FlyBase ID | FBal0215824 | |
| Feature type | allele | Associated gene | Dmel\Dscam |
| Allele class | |||
| Mutagen | recombination, FLPase, gene targeting by homologous recombination | ||
Recent Updates
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| Description |
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| FB2013_03 | |||
| FB2013_02 | |||
| All updates | Click here to see a list of all updates to this record from FB2010_08 and on. | ||
Nature of the Allele
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| Allele class | |||
| Mutagen | |||
| Mutations Mapped to the Genome | |||
Type Location Additional Notes References | |||
| Associated Sequence Data | |||
| DDBJ
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EMBL / GenBank | DNA sequence Protein sequence Name | ||
| UniProtKB/Swiss-Prot | |||
| UniProtKB/TrEMBL | |||
| Progenitor genotype | |||
| Nature of the lesion | Statement Reference Recombination between the single Scer\FRT sites that are present on each of Dp(2;2)DscamED69 and Dp(2;2)Dscam5'HR-3.31.8 has resulted a single copy of Dscam in which the genomic region encoding exons 3 to 16 has been replaced with cDNA sequences. This copy of Dscam encodes a single ectodomain isoform, containing the variable exons 4.3, 6.31 and 9.8. A single Scer\FRT site is present following the cDNA sequences. Homologous recombination has been used to replace the genomic region encoding the variable ectodomains with cDNA sequences encoding a single isoform, which in this case contains the variable exons 4.3, 6.31 and 9.8. A single Scer\FRT site is inserted in the intron between exons 16 and 17. | ||
| Cytology | |||
Phenotypic Data
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Phenotypic Class
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Phenotype Manifest In
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Detailed Description
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Statement Reference Homozygotes, Dscam10.27.25/Dscam3.31.8 and Dscam3.31.8/Dscam6.5.9 animals die in early larval development.
Over 75% of Dscam3.31.8/Dscam23 animals survive to late pupal stages.
Homozygous, Dscam10.27.25/Dscam3.31.8 and Dscam3.31.8/Dscam6.5.9 embryos show defects in the organisation of the central nervous system, showing severely disrupted longitudinal tracts and aberrant midline crossing.
Dscam3.31.8/Dscam23 embryos show defects in the organisation of the central nervous system, showing disrupted longitudinal tracts.
Dscam3.31.8/Dscam- animals have a highly disorganised antennal lobe with no distinct glomerular structure and olfactory receptor neurons form many ectopic termini throughout the antennal lobe.
Almost all Dscam3.31.8/Dscam- mushroom bodies completely lack one lobe (typically the dorsal lobe is missing). Dscam3.31.8/+ animals also show defects in the mushroom body in approximately 90% of cases; either one mushroom body lobe is absent (approximately 60% of cases) or one mushroom body lobe is thinner than the other (approximately 30% of cases).
Sister branches of single Dscam3.31.8 mushroom body neurons in a DscamFRT control background (generated using intragenic MARCM) segregate into the two mushroom body lobes with high fidelity. | |||
External Data
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Interactions
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Phenotypic Class
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Phenotype Manifest In
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Additional Comments
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Genetic Interactions
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Statement Reference | |||
Xenogenetic Interactions
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Statement Reference | |||
Complementation & Rescue Data
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| Comments | |||
Stocks
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Notes on Origin
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| Discoverer | |||
External Crossreferences & Linkouts
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Synonyms & Secondary IDs
( 1 ) | |||
| Reported As | |||
| Symbol Synonym | Dscam3.31.8 | ||
| Name Synonym | |||
| Secondary FlyBase IDs | |||
References
( 2 ) | |||
| Research paper |
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| Supplementary material |
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Recent Updates
External Crossreferences & Linkouts