Aberration Dmel\Df(2R)M41A4
| General Information | |||
|---|---|---|---|
| Symbol | Dmel\Df(2R)M41A4 | Species | D. melanogaster |
| Name | Deficiency (2R) Minute 41A | FlyBase ID | FBab0001993 |
| Feature type | chromosomal_deletion | ||
| Computed Breakpoints include | h44-h46;42A1-42A2 | ||
| Deleted segment | h44--42A2 | ||
| Sequence coordinates | |||
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| Description |
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| FB2012_01 | |||
| FB2011_10 | |||
| 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 | 41A;41A 41A;[] 41C;42A1-42A2 [];42A1--2 [];h46 | ||
| Causes alleles | |||
| Carries alleles | |||
| Transposon Insertions | |||
| Formalized genetic data | uex << bk1 << RpL38 << ap << bk2 << mle | ||
| Genetic mapping information | |||
| Comments | |||
Comments on Cytology
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Euchromatic breakpoint not reported. Left limit of break 1 from non-inclusion of uex (FBrf0028786) Right limit of break 1 from inclusion of l(2)41Ae (FBrf0027524) Limits of break 2 from polytene analysis (FBrf0091444) | |||
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)M41A10. | ||
| NOT in combination with other aberrations | Does not cause unconditional lethality in hybrid females when heterozygous with D.simulans chromosome. Weak second site non-complementing phenotype with zipEbr and zipmhc-c6.1: malformed phenotype penetrance 10-24%. Shows no maternal enhancement of dpphr4. Midgut development of mutant embryos is wild type. Homozygous embryos are very abnormal compared to wild-type. Formation of the gut is variable. Heterozygosity for this deletion has no effect on the mutant ovarian phenotype of ovoD2. Heterozygotes show a Minute phenotype. Homozygous lethal. homozygous lethal Medium Minute bristles. Large pale body with heavy, malformed, bloated abdomen. Female fertility low. | ||
Stocks
( 3 ) | |||
| Bloomington | |||
| Kyoto | 108912 | ||
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(2R)M41A4 chromosome acts as a dominant weak 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
( 21 ) | |||
| Reported As | |||
| Symbol Synonym | 41A4 Df(2)M-S4 Df(2R)M41 Df(2R)m41A4 Df(2R)M41A4 Df(2R)M-S2-4 Df(2R)MS2-4 Df(2R)M-S24 Df(2R)MS24 Df(2R)M-S4 Df(2R)MS24 DfMS4 M41A4 M(2)S24 M(2)S4 M(2)S-4 M(2R)S24 MS2-4 M-S24 | ||
| Name Synonym | Deficiency (2R) Minute 41A | ||
| Secondary FlyBase IDs | |||
References
( 56 ) | |||
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Recent research papers (0)
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| All research papers listed in FlyBase were published before 2010 | |||
Recent reviews (0)
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| All reviews listed in FlyBase were published before 2010 | |||
Recent Updates