Aberration Dmel\Df(2R)CX1
| General Information | |||
|---|---|---|---|
| Symbol | Dmel\Df(2R)CX1 | Species | D. melanogaster |
| Name | FlyBase ID | FBab0022242 | |
| Feature type | chromosomal_deletion | Created / Updated | 2006-08-22/2006-08-22 |
| Formalized genetic data | stil << bk1 << E(Egfr)B56 << mam << bk2 | ||
| Sequence coordinates | |||
| Deleted segment | 49C1--50D1 | ||
| Duplicated segment | |||
| Computed Breakpoints include | 49C1-49C4;50C23-50D1 | ||
| Breakpoints Inherited | |||
Nature of the Aberration
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| Cytological Order | |||
| Progenitor | |||
| Mutagen | |||
| Class of aberration (relative to progenitor) | |||
| Breakpoints | 49C1-49C4;50C23-50D2 49D1;50C23-50D1 | ||
| Causes alleles | |||
| Carries alleles | |||
| Transposon Insertions | |||
| Genetic mapping information | |||
| Comments | |||
Comments on Cytology
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Limits of break 1 from polytene analysis (FBrf0080145) Left limit of break 2 from polytene analysis (FBrf0080145) Right limit of break 2 from polytene analysis (FBrf0091150) Ref: Mlodzik et al., 1990, Genes Dev. 4: 1848--1861 Deletion of the site of P{lacW}50C repeat arrays inserted at 50C10-50C14. | |||
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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Df(2R)CX1 fails to complement the P{lacW}Nrkk14301 insertion line ("l(2)k14301"). | |||
Phenotypic Data
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| In combination with other aberrations | |||
| NOT in combination with other aberrations | Causes inviability or low viability in hybrid females when heterozygous with D.simulans chromosome. Complementation tests with E(Egfr)B56B56 reveal defects in wing vein L2, L4 and L5. Midgut development of mutant embryos is wild type. Weak second site non-complementing phenotype with zipEbr and zipmhc-c6.1: malformed phenotype penetrance 10-24%. | ||
Position Effect Variegation Data
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Stocks
( 3 ) | |||
| Kyoto | 108903 103277 | ||
| Bloomington | |||
Notes on Origin
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| Discoverer | N. Baker. | ||
Separable from: wg12. | |||
Balancer / Genotype Variants of the Aberration
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Separable Components
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Other Comments
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The Df(2R)CX1 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 assumed to be a false positive result (the suppressor may not be within the bounds of the deficient region) because the 2L TAS array on the chromosome is reduced (as assayed by in situ hybridization) and it has previously been shown (FBrf0137248, FBrf0158986) that partial or complete deficiency of the 2L TAS array on the homologue suppresses silencing of brown-red variants of P{3'WP-2,wvar}2Lt. | |||
Synonyms & Secondary IDs
( 5 ) | |||
| Reported As | |||
| Symbol Synonym | Df(2L)CX1 Df(2R)CX Df(2R)CX1 | ||
| Name Synonym | |||
| Secondary FlyBase IDs | |||
References
( 53 ) | |||
| Generate a list of | |||
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Recent research papers ( 2 ) | |||
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Nature of the Aberration