Aberration Dmel\Df(2L)b87e25
| General Information | |||
|---|---|---|---|
| Symbol | Dmel\Df(2L)b87e25 | Species | D. melanogaster |
| Name | Deficiency (2L) black | FlyBase ID | FBab0001747 |
| Feature type | chromosomal_deletion | Created / Updated | 2006-08-22/2006-08-22 |
| Formalized genetic data | bk1 << kuz << vas << bk2 << stc | ||
| Sequence coordinates | |||
| Deleted segment | 34C1--35C1 | ||
| Duplicated segment | |||
| Computed Breakpoints include | 34C1;35C1 | ||
| Breakpoints Inherited | |||
Nature of the Aberration
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| Cytological Order | |||
| Progenitor | |||
| Mutagen | |||
| Class of aberration (relative to progenitor) | |||
| Breakpoints | 34C1;35C1-35C2 34B12-34C1;35B10-35C1 34D3;35B10 34C1-34C2;35B10-35C1 | ||
| Causes alleles | |||
| Carries alleles | |||
| Transposon Insertions | |||
| Genetic mapping information | |||
| Comments | |||
Comments on Cytology
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Limits of break 1 from polytene analysis (FBrf0053558) Left limit of break 2 from inclusion of vas (FBrf0077941) Right limit of break 2 from polytene analysis (FBrf0080145) Ref: Lindsley and Zimm, 1992 | |||
Molecularly Mapped Breakpoints
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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 | |||
| NOT in combination with other aberrations | Df(2L)b87e25 in combination with a pair of introgressions from D.simulans spanning 30F1-31E7 to 35D7-36A14 Dsim\Int(2L)S and 21A1 to 22D1--23A2 Dsim\Int(2L)D produces semi-sterile male flies. These flies are female sterile. Deficient embryos show an uninterpretable mutant midgut phenotype. Homozygous embryos are very abnormal compared to wild-type. Lethal in combination with: Df(2L)BSC147. Inferred to overlap with: Df(2L)BSC147. No second site non-complementing phenotype with zipEbr and zipmhc-c6.1. Shows no maternal enhancement of dpphr4. Suppresses the ommatidial polarity phenotype of dshhs.sev.B. Suppresses the ommatidial polarity phenotype of msnEP549 when driven by Scer\GAL4hs.2sev. | ||
Position Effect Variegation Data
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Stocks
( 3 ) | |||
| Bloomington | 3138 | ||
| Kyoto | 106874 | ||
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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"irradiation" was stated as tentative. "spontaneous" was stated as tentative. The Df(2L)b87e25 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), but this is a false positive result (the suppressor is not within the bounds of the deficient region) because the suppressor maps to the tip of 2L rather than to the site of the deficiency. In addition, the deficiency chromosome fails to complement lethal mutations of l(2)gl. | |||
Synonyms & Secondary IDs
( 9 ) | |||
| Reported As | |||
| Symbol Synonym | 3138 Df(2L)87e25 Df(2L)b80e25 Df(2L)b87E25 Df(2L)b87e25 Df(2L)b87e35 | ||
| Name Synonym | Deficiency (2L) black | ||
| Secondary FlyBase IDs | |||
References
( 34 ) | |||
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Recent research papers ( 1 ) | |||
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Nature of the Aberration