Aberration Dmel\Df(2L)E55
| General Information | |||
|---|---|---|---|
| Symbol | Dmel\Df(2L)E55 | Species | D. melanogaster |
| Name | FlyBase ID | FBab0001458 | |
| Feature type | chromosomal_deletion | ||
| Computed Breakpoints include | 37D2;38A1 | ||
| Deleted segment | 37D2--38A1 | ||
Map ( GBrowse )
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ErrorNo matching regions found. | ||
| Sequence coordinates | 2L:19,691,199..19,701,224 [+] (Df(2L)E55:bk2) | ||
| 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 | 37C6-37D1;37F5-38A1 37D2-37E1;35F5-38A1 37D2-37E1;37F5-38A1 | ||
| Causes alleles | |||
| Carries alleles | |||
| Transposon Insertions | |||
| Formalized genetic data | γTub37C << bk1 << l(2)37Da << fs(2)lto3 << bk2 << Lar | ||
| Genetic mapping information | |||
| Comments | Breakpoint(s) molecularly mapped | ||
Comments on Cytology
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Left limit of break 1 from polytene analysis (FBrf0028752) Right limit of break 1 from inclusion of l(2)37Da (citation unavailable) Left limit of break 2 from inclusion of Lar (FBrf0086508) Right limit of break 2 from polytene analysis (FBrf0028752) | |||
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 | Fails to complement Df(2L)Exel9043. No effect on In(1)wm4h position-effect variegation. Lethal over Df(2L)TW9 and Df(2L)TW158. Df(2L)E55/Df(2L)TW330 lethal Df(2L)E55/Df(2L)VA15 lethal Df(2L)E55/Df(2L)VA20 lethal Df(2L)E55/Df(2L)VA22 lethal Df(2L)E55/Df(2L)VA23 lethal Df(2L)E55/Df(2L)VA25 lethal Df(2L)E55/Df(2L)TW9 lethal Df(2L)E55/Df(2L)TW12 lethal Df(2L)E55/Df(2L)TW150 viable Df(2L)E55/Df(2L)TW84 viable Df(2L)E55/Df(2L)OD16 viable Df(2L)E55/Df(2L)TW150 non-transparent wing phenotype Df(2L)E55/Df(2L)TW84 non-transparent wing phenotype Df(2L)E55/Df(2L)OD16 non-transparent wing phenotype | ||
| NOT in combination with other aberrations | Shows no maternal enhancement of dpphr4. The central nervous system (CNS) is narrower than normal and the commissures are thicker than normal and incompletely separated in Df(2L)E55 embryos. Dominantly causes tergite defects in less than 50% of run3 heterozygotes. Midgut development of mutant embryos is wild type. Homozygous embryos do not always complete head involution. Heterozygosity for this deletion suppresses the mutant ovarian phenotype of ovoD2. | ||
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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The Df(2L)E55 chromosome acts as a dominant moderate 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 region of the deficiency is covered by one or more nonsuppressing deficiencies. | |||
Synonyms & Secondary IDs
( 4 ) | |||
| Reported As | |||
| Symbol Synonym | Df(2L)TWE55 Df(3L)E55 | ||
| Name Synonym | |||
| Secondary FlyBase IDs | |||
References
( 44 ) | |||
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Recent research papers (0)
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| All research papers listed in FlyBase were published before 2011 | |||

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