Aberration Dmel\Df(2L)BSC41
| General Information | |||
|---|---|---|---|
| Symbol | Dmel\Df(2L)BSC41 | Species | D. melanogaster |
| Name | FlyBase ID | FBab0037635 | |
| Feature type | chromosomal_deletion | ||
| Computed Breakpoints include | |||
| Deleted segment | 28A4--28D9 | ||
| Sequence coordinates | |||
| Member of large scale dataset(s) | A set of ~50 targeted deficiencies created by exploiting hybrid element insertion (HEI) and resolution; designed to fill gaps in deletion coverage. | ||
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 Aberration
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| Cytological Order | |||
| Progenitor | |||
| Mutagen | |||
| Class of aberration (relative to progenitor) | |||
| Breakpoints | 28A4-28B1;28D3-28D9 | ||
| Causes alleles | |||
| Carries alleles | |||
| Transposon Insertions | |||
| Formalized genetic data | |||
| Genetic mapping information | |||
| Comments | Inverse PCR experiments using the Df(2L)BSC41 chromosome indicate that neither of the progenitor insertions (P{lacW}l(2)k05404k05404 and P{EP}EP946) remains in its original position, neither of the elements is intact and both insertions made jumps during the mobilisation scheme used to make Df(2L)BSC41. The proximal breakpoint is approximately 30kb proximal to the P{EP}EP946 insertion point. | ||
Comments on Cytology
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Sequence Crossreferences
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| DDBJ
/
EMBL / GenBank | DNA sequence Protein sequence Name | ||
Gene Deletion & Duplication Data
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Genes Deleted / Disrupted
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| Complementation Data | |||
| Completely deleted / disrupted | |||
| Molecular Data | |||
Genes NOT Deleted / Disrupted
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| Complementation Data | |||
| Molecular Data | |||
Genes Duplicated
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| Complementation Data | |||
| Molecular Data | |||
Genes NOT Duplicated
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| Complementation Data | |||
| Molecular Data | |||
Related Comments
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Phenotypic Data
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| In combination with other aberrations | |||
| NOT in combination with other aberrations | |||
Stocks
( 2 ) | |||
| Bloomington | |||
| Kyoto | |||
Notes on Origin
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| Discoverer | |||
Balancer / Genotype Variants of the Aberration
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Separable Components
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Other Comments
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The deletion chromosome retained one or both mini-white markers from the P{lacW} and P{EP}EP1090 insertions used in the screen. | |||
Synonyms & Secondary IDs
( 1 ) | |||
| Reported As | |||
| Symbol Synonym | Df(2L)BSC41 | ||
| Name Synonym | |||
| Secondary FlyBase IDs | |||
References
( 7 ) | |||
| Research paper |
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| Supplementary material |
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| Personal communication to FlyBase |
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| FlyBase analysis |
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Recent Updates