Aberration Dmel\In(2LR)Px4
| General Information | |||
|---|---|---|---|
| Symbol | Dmel\In(2LR)Px4 | Species | D. melanogaster |
| Name | Inversion (2LR) Plexate | FlyBase ID | FBab0004789 |
| Feature type | chromosomal_inversion | Created / Updated | 2006-08-22/2006-08-22 |
| Formalized genetic data | |||
| Sequence coordinates | |||
| Deleted segment | |||
| Duplicated segment | |||
| Computed Breakpoints include | |||
| Breakpoints Inherited | |||
Nature of the Aberration
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| Cytological Order |
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| Progenitor | |||
| Mutagen | |||
| Class of aberration (relative to progenitor) | |||
| Breakpoints | |||
| Causes alleles | |||
| Carries alleles | |||
| Transposon Insertions | |||
| Genetic mapping information | |||
| Comments | |||
Comments on Cytology
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Inverted for 60B8-60B10;60D1 Deficient for 60B-60C;60D1-60D2 | |||
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 | |||
| Completely duplicated | |||
| 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 | Heterozygotes have a blistered wing and ectopic vein phenotype. Heterozygotes with T(2;3)God1 are inviable. Homozygotes die at the beginning of the first larval instar stage because the larvae cannot exit from the chorion. The larvae are deformed with stunted growth. The sclerotised mouthparts and denticle belts develop normally. Intermediate second site non-complementing phenotype with zipEbr and zipmhc-c6.1: malformed phenotype penetrance 25-75%. Midgut development of mutant embryos is wild type. Progeny of the genotype zip/Df(zip) exhibit the mlf phenotype (malformed syndrome), wing malformations and leg defects, at a penetrance of 14--35%. Shows a haploinsufficient ectopic wing vein phenotype. Shows no maternal enhancement of dpphr4. The tracheal phenotypes previously reported for this deficiency in FBrf0051997 and FBrf0072461, where the primary branches are disrupted and discontinuous, are due to the deletion of a gene other than bs, or more than one gene in the region. Wing venation phenotype like Df(2R)Px1. Thickening of L5 at posterior crossvein produces a vesicle, as in bs. More extreme in female. homozygous lethal | ||
Position Effect Variegation Data
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Stocks
( 3 ) | |||
| Bloomington | |||
| Kyoto | 106331 | ||
Notes on Origin
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| Discoverer | Thompson, June 1956, 1957. | ||
A recurrent product of recombination in region 33F-40F between In(2LR)21C8-D1;60D1-2 from In(2LR)bwV1 [In(2LR)21C8-D1;60D1-2 + In(2LR)40F;59D4-E1] and In(2LR)22A3-B1;60B-C from SM1 [In(2L)Cy = In(2L)22D1-2;33F5-34A1 + In(2LR)22A3-B1;60B-C + In(2R)Cy = In(2R)42A2-3;58A4-B1]. | |||
Balancer / Genotype Variants of the Aberration
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Separable Components
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Other Comments
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"Deletes or disrupts sp" was stated as tentative. The reciprocal recombinant is In(2LR)S56f. | |||
Synonyms & Secondary IDs
( 13 ) | |||
| Reported As | |||
| Symbol Synonym | BL-1473 Df(2LR)Px4 Df(2R)Px1 Df(2R)Px4 Df(2R)Px4,Dp(2L) Df(2R)Px[4] Df(2R)Px4 Dp(2;2)S56f In(2LR)Px4 In(2LR)Px4 In(2R)Px4 Px4 | ||
| Name Synonym | Inversion (2LR) Plexate | ||
| Secondary FlyBase IDs | |||
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References
( 37 ) | |||
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Recent research papers ( 1 ) | |||
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Nature of the Aberration