Aberration Dmel\Df(2L)TW65
| General Information | |||
|---|---|---|---|
| Symbol | Dmel\Df(2L)TW65 | Species | D. melanogaster |
| Name | Deficiency (2L) Ted Wright | FlyBase ID | FBab0001656 |
| Feature type | chromosomal_deletion | ||
| Also Known As | Df(2L)65 | ||
| Computed Breakpoints include | 38A1;39F1 | ||
| Deleted segment | 38A1--39F1 | ||
| Sequence coordinates | |||
| Member of large scale dataset(s) | |||
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 | 37F5-38A1;38B2-38C1 37F5-38A1;39E2-39F1 | ||
| Causes alleles | |||
| Carries alleles | |||
| Transposon Insertions | |||
| Formalized genetic data | l(2)37Fe << bk1 << Fs(2)Ket << l(2)39Ea << bk2 << M(2)39F | ||
| Genetic mapping information | |||
| Comments | |||
Comments on Cytology
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Left limit of break 1 from non-inclusion of l(2)37Fe (citation unavailable) Right limit of break 1 from inclusion of l(2)37Fg (FBrf0058099) Left limit of break 2 from inclusion of l(2)03832a (FBrf0067338) Right limit of break 2 from polytene analysis (FBrf0080317) | |||
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 | |||
| Partially 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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Partially complements l(2)39DEhD95, l(2)39DElK234, l(2)39DEmK236, l(2)39DEnL110, l(2)39DEoL138 and l(2)39DEiD241. | |||
Phenotypic Data
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| In combination with other aberrations | |||
| NOT in combination with other aberrations | The Df(2L)TW65 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 this deletion has no effect on the mutant ovarian phenotype of ovoD2. Replication ceased midway through the extended germ band stage, gut does not form and there is no evidence of patterning in the epidermis. | ||
Stocks
( 2 ) | |||
| Bloomington | 1602 | ||
| Kyoto | 106411 | ||
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 | 65 Df(2L)TW65 TW65 | ||
| Name Synonym | Deficiency (2L) Ted Wright | ||
| Secondary FlyBase IDs | |||
References
( 35 ) | |||
| Generate a list of | |||
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Recent research papers (0)
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| All research papers listed in FlyBase were published before 2011 | |||
Recent Updates