Allele Dmel\aope2d
| General Information | |||
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| Symbol | Dmel\aope2d | Species | D. melanogaster |
| Name | FlyBase ID | FBal0049301 | |
| Feature type | allele | Associated gene | Dmel\aop |
| Also Known As | yane2D | ||
| Allele class | amorphic allele - genetic evidence | ||
| Mutagen | |||
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 Allele
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| Allele class | |||
| Mutagen | |||
| Mutations Mapped to the Genome | |||
Type 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 | ||
| Cytology | |||
Phenotypic Data
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Phenotypic Class
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Phenotype Manifest In
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ommatidium (with aoppok-x8) pigment cell (with aoppok-x8) | |||
Detailed Description
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Statement Reference aop[yan-1]/aop[e2d] eye discs show chirality defects in ommatidial clusters. | |||
External Data
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| Linkouts | |||
Interactions
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Phenotypic Class
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Enhancer of | |||
Statement Reference aop[+]/aope2d is an enhancer of planar polarity defective phenotype of Scer\GAL4hs.2sev, dgoScer\UAS.cFa | |||
Suppressor of | |||
Statement Reference | |||
Other | |||
Statement Reference | |||
Phenotype Manifest In
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Enhancer of | |||
Statement Reference | |||
NOT Enhancer of | |||
Statement Reference | |||
Suppressor of | |||
Statement Reference | |||
NOT Suppressor of | |||
Statement Reference | |||
Other | |||
Statement Reference | |||
Additional Comments
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Genetic Interactions
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Statement Reference aop[e2d]/+ enhances the planar cell polarity (PCP) defects in the eye induced by the overexpression of dgo[Scer\UAS.cFa] under the control of Scer\GAL4[hs.2sev]. Homozygous kay[2] clones in the eye in a aop[e2d]/+ background show ommatidial chirality, rotation and photoreceptor number defects (kay[2] single mutant clones do not show tissue polarity defects by themselves).
One copy of aop[e2d] partially suppresses the formation of symmetrical ommatidia that is seen in animals expressing dsh[hs.sev.B]. Loss of wild type ttk promotes the formation of rare ectopic R7 cells. Heterozygotes with aoppok-x8 or aopyan-1 are semi-lethal and the adult escapers have small rough eyes due to fusion of ommatidia, loss of the regular pigment cell array and ectopic R7 cells. sev6/sev+;SosJC2/aope2d mutants exhibit an increase in the number of R7 cells compared to sev6/SosJC2 mutants with two functional aop copies. | |||
Xenogenetic Interactions
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Statement Reference | |||
Complementation & Rescue Data
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| Partially complements | |||
| Fails to complement | |||
| Comments | |||
Stocks
( 0 ) | |||
Notes on Origin
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| Discoverer | |||
External Crossreferences & Linkouts
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| Other Crossreferences | |||
| Linkouts | |||
Synonyms & Secondary IDs
( 6 ) | |||
| Reported As | |||
| Symbol Synonym | aope2d aopE2d e2d yane2D yane2d yanE2d | ||
| Name Synonym | |||
| Secondary FlyBase IDs | |||
References
( 9 ) | |||
| Research paper |
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Recent Updates
External Crossreferences & Linkouts