Aberration Dmel\Df(2L)TW137
| General Information | |||
|---|---|---|---|
| Symbol | Dmel\Df(2L)TW137 | Species | D. melanogaster |
| Name | Deficiency (2L) Ted Wright | FlyBase ID | FBab0001645 |
| Feature type | chromosomal_deletion | Created / Updated | 2006-08-22/2006-08-22 |
| Formalized genetic data | l(2)36Bd << bk1 << l(2)36Ca << pre << bk2 << hk | ||
| Sequence coordinates | |||
| Deleted segment | 36C2--37B10 | ||
| Duplicated segment | |||
| Computed Breakpoints include | 36C2-36C4;37B9-37B10 | ||
| Breakpoints Inherited | |||
Nature of the Aberration
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| Cytological Order | |||
| Progenitor | |||
| Mutagen | |||
| Class of aberration (relative to progenitor) | |||
| Breakpoints | 36C2-36C4;37B9-37C1 | ||
| Causes alleles | |||
| Carries alleles | |||
| Transposon Insertions | |||
| Genetic mapping information | |||
| Comments | Distal DNA breakpoints given (Steward, McNally, and Schedl, 1984, Nature 311: 262-65) | ||
Comments on Cytology
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Limits of break 1 from polytene analysis (FBrf0028752) Left limit of break 2 from polytene analysis (FBrf0028752) Right limit of break 2 from non-inclusion of Catsup (FBrf0084402) | |||
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)TW137 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 fertile male flies. These flies are female sterile. Does not cause unconditional lethality in hybrid females when heterozygous with D.simulans chromosome. Heterozygosity for Df(2L)TW137 results in 1.0% X chromosome nondisjunction and 0.0% fourth chromosome nondisjunction in In(1)FM7/X ; svspa-pol females. Heterozygosity for this deletion has no effect on the mutant ovarian phenotype of ovoD2. Moderate Minute. No second site non-complementing phenotype with zipEbr and zipmhc-c6.1. The Df(2L)TW137 chromosome does not act as a dominant 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). | ||
Position Effect Variegation Data
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Stocks
( 3 ) | |||
| 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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Synonyms & Secondary IDs
( 5 ) | |||
| Reported As | |||
| Symbol Synonym | Df(2L)137 Df(2L)TW137 Df-TW137 TW137 | ||
| Name Synonym | Deficiency (2L) Ted Wright | ||
| Secondary FlyBase IDs | |||
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References
( 45 ) | |||
| Generate a list of | |||
| List References by type |
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Recent research papers ( 1 ) | |||
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Nature of the Aberration