|Name||Deficiency (3R) stubbloid||FlyBase ID||FBab0002924|
|Also Known As||Df(3R)sbd26|
|Computed Breakpoints include||89B9;89C7|
|Member of large scale dataset(s)|
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|Nature of the Aberration|
|Class of aberration (relative to progenitor)|
|Formalized genetic data||Akt1 << bk1 << sra << bk2 << Abd-B|
|Genetic mapping information|
|Comments on Cytology|
The sbd phenotype and the deficiency are probably independent. The proximal breakpoint of the deficiency maps at least 112kb away from the nearest part of the transcript.
|Gene Deletion & Duplication Data|
|Genes Deleted / Disrupted|
|Completely deleted / disrupted|
|Genes NOT Deleted / Disrupted|
|Genes NOT Duplicated|
|In combination with other aberrations|
Df(3R)sbd26/Df(3R)sbd105 transheterozygote gives viable malformed escapers, but the 'sbd26' mutation may be independent of the deficiency.
Df(3R)sbd26/In(3R)sbd17 viable Df(3R)sbd26/In(3R)sbd17 sbd phenotype Df(3R)sbd26/In(3R)sbd12 lethal with adult escapers that are sbd Df(3R)sbd26/sbd13 lethal with adult escapers that are sbd Df(3R)sbd26/sbd18 and lethal with adult escapers that are sbd Df(3R)sbd26/In(3R)sbd21 lethal with adult escapers that are sbd
|NOT in combination with other aberrations|
|Stocks ( 3 )|
|Notes on Origin|
|Balancer / Genotype Variants of the Aberration|
|Synonyms & Secondary IDs ( 5 )|
Deficiency (3R) stubbloid
|Secondary FlyBase IDs|
|References ( 23 )|
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|Recent research papers (0)|
|All research papers listed in FlyBase were published before 2011|