Aberration Dmel\Df(3L)BSC13
| General Information | |||
|---|---|---|---|
| Symbol | Dmel\Df(3L)BSC13 | Species | D. melanogaster |
| Name | FlyBase ID | FBab0029723 | |
| Feature type | chromosomal_deletion | ||
| Computed Breakpoints include | |||
| Deleted segment | 66B12--66D4 | ||
| 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. | ||
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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 | 66B12-66C1;66D2-66D4 66B12-66C14;66D2-66D4 | ||
| Causes alleles | |||
| Carries alleles | |||
| Transposon Insertions | |||
| Formalized genetic data | |||
| Genetic mapping information | |||
| Comments | |||
Comments on Cytology
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Sequence Crossreferences
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| DDBJ
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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 | Lethal in combination with T(2;3)E(da). | ||
| NOT in combination with other aberrations | The distal half of the salivary gland turns but the proximal half does not in embryos homozygous for Df(3L)BSC13 by stage 14. The Df(3L)BSC13 chromosome acts as a dominant weak suppressor of telomeric silencing (assayed using the effect of the chromosome on the eye colour phenotype of flies carrying "P{wvar}KR3-2", a stable "brown-red" variant of the P{3'WP-2,wvar}2Lt insertion). Heterozygosity for Df(3L)BSC13 results in 50.8% X chromosome nondisjunction and 11.9% fourth chromosome nondisjunction in In(1)FM7/X ; svspa-pol females. | ||
Stocks
( 1 ) | |||
| 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 miniwhite markers from both P{lacW}Nmtj1C7 and P{EP}ergic53EP3212 were deleted or disrupted. | |||
Synonyms & Secondary IDs
( 1 ) | |||
| Reported As | |||
| Symbol Synonym | |||
| Name Synonym | |||
| Secondary FlyBase IDs | |||
References
( 15 ) | |||
| Research paper |
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| Supplementary material |
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| Erratum |
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| Personal communication to FlyBase |
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| FlyBase analysis |
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Recent Updates