Allele Dmel\Egfrf5
| General Information | |||
|---|---|---|---|
| Symbol | Dmel\Egfrf5 | Species | D. melanogaster |
| Name | FlyBase ID | FBal0003533 | |
| Feature type | allele | Created / Updated | 2006-08-22/2006-08-22 |
| Associated gene | Dmel\Egfr | ||
| Allele class | amorph, hypomorph | ||
| Mutagen | ethyl methanesulfonate | ||
Nature of the Allele
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| Allele class | |||
| Mutagen | |||
| Mapped Features and Mutations | |||
Type Symbol & Location Additional Notes References | |||
| Associated Sequence Data | |||
| DDBJ
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EMBL / GenBank | DNA sequence Protein sequence Name | ||
| UniProtKB/Swiss-Prot | |||
| UniProtKB/TrEMBL | |||
| Progenitor genotype | |||
| Nature of the lesion | Statement Reference Nucleotide substitution: G926A. Amino acid replacement: W186@. Stop codon is an amber. | ||
| Assay mode | |||
| Cytology | |||
Phenotypic Data
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Phenotypic Class
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Phenotype Manifest In
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Detailed Description
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Statement Reference severe allele Homozygotes and hemizygotes display an intermediate 'flb' phenotype. Embryos produced from heteroallelic combination with Egfrt1 have a severe ventralised phenotype, reduction in size of their dorsal appendage. Enhances the female sterility and adult morphological defects of Egfrt1. Rarely survives as transheterozygote with the semi-viable Egfrtop-CA allele. In mutant embryos, massive cell death occurs in the head. The visual system is almost entirely absent, though the Bolwig's organ remains. Egfrf5 stage 11 embryos show domains of cell death in the anterior and posterior parts of the head. The posterior domain covers the optic placode. The apoptosis results in loss of major portions of the head epidermis, so that the brain is exposed in stage 14 embryos. The optic placode has almost disappeared by stage 14. The apoptosis is delayed in the optic placode relative to the apoptosis in the head epidermis. Cell death is also seen in the ventral neuroectoderm at stage 10/11. Late stage mutant embryos show a strong reduction in size of the corpus cardiacum compared to wild type and the stomatogastric nervous system is absent. | |||
Interactions
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Phenotypic Class
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Phenotype Manifest In
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Suppressed by | |||
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NOT suppressed by | |||
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Suppressor of | |||
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Other | |||
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Additional Comments
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Genetic Interactions
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Statement Reference The optic lobes are restored in double mutants with Df(3L)H99. The optic placode fails to invaginate in Egfrf5 ; Df(3L)H99 embryos, leaving it exposed at the surface of the embryo. Cells that would normally separate from the placode and become the Bolwig's organ remain part of the placode. These cells show a typical epithelial phenotype and are structurally indistinguishable from the surrounding optic lobe cells (although they express neuronal markers). In some cases, outgrowth of short, axon-like processes is seen. | |||
Xenogenetic Interactions
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Complementation & Rescue Data
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Stocks
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Notes on Origin
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| Discoverer | |||
Selected as: Embryonic lethal. | |||
Comments
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Mutation of Egfr that coordinately affects all gene activities, a class I lesion. The allelic series for class I lesions: Egfrt2 = Egfrt1 < Egfrtop-EC20 < Egfrf7 = Egfrf1 = Egfrflb-2E07 < Egfrtop-EE39 = Egfrtop-ED26 = Egfrf5 < Egfrf9 = Egfrf10 = Egfrf2 = Egfrtop-EE42 = Egfrf11 = Egfrf24 = Egfrf3 = Df(2R)Egfr3. Class I allele. | |||
Synonyms & Secondary IDs
( 6 ) | |||
| Reported As | |||
| Symbol Synonym | Egfrf5 flb flb2G31 | ||
| Name Synonym | faint little ball | ||
| Secondary FlyBase IDs | |||
References
( 14 ) | |||
| Research paper |
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| Stock list |
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Nature of the Allele