Aberration Dmel\Df(2R)X1
| General Information | |||
|---|---|---|---|
| Symbol | Dmel\Df(2R)X1 | Species | D. melanogaster |
| Name | FlyBase ID | FBab0002048 | |
| Feature type | chromosomal_deletion | ||
| Computed Breakpoints include | 46C2;47A1 | ||
| Deleted segment | 46C2--47A1 | ||
Map ( GBrowse )
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ErrorNo matching regions found. | ||
| Sequence coordinates | 2R:5,809,508..5,814,962 [-] (Df(2R)X1:bk1) | ||
| 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 | 46C;46E-46F 46C;46F 46C;47A1 | ||
| Causes alleles | |||
| Carries alleles | |||
| Transposon Insertions | |||
| Formalized genetic data | bk1 hits Mef2 << Syb << bk2 | ||
| Genetic mapping information | |||
| Comments | |||
Comments on Cytology
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Proximal breakpoint is 15-20kb distal to Fmrf. Complementation data from unspecified deficiency chromosomes. Left limit of break 1 from non-inclusion of Fmrf (FBrf0053296) Right limit of break 1 from inclusion of Mef2 (FBrf0078093) Limits of break 2 from polytene analysis (FBrf0058167) | |||
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 | Lethal in combination with Df(2R)12. | ||
| NOT in combination with other aberrations | The Df(2R)X1 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). Heterozygosity for this deletion has no effect on the mutant ovarian phenotype of ovoD2. | ||
Stocks
( 2 ) | |||
| 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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Complementation group identified in an EMS and DEB screen to isolate deficiencies that uncover Jra. | |||
Synonyms & Secondary IDs
( 6 ) | |||
| Reported As | |||
| Symbol Synonym | Df(2)X1 DF(2R)X1 Df(2R)X1 l(2)46CFw unnamed | ||
| Name Synonym | |||
| Secondary FlyBase IDs | |||
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References
( 49 ) | |||
| Generate a list of | |||
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Recent research papers ( 2 ) | |||
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Recent Updates