Allele Dmel\Atg2EP3697
| General Information | |||
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| Symbol | Dmel\Atg2EP3697 | Species | D. melanogaster |
| Name | FlyBase ID | FBal0123243 | |
| Feature type | allele | Associated gene | Dmel\Atg2 |
| Map ( GBrowse ) |
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| Allele class | |||
| Mutagen | P-element activity | ||
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 transposable element insertion site | |||
| 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 | ||
| Caused by insertion | |||
| Cytology | |||
Phenotypic Data
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Phenotypic Class
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Phenotype Manifest In
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anterior fascicle & synapse, with Scer\GAL4elav-C155 | |||
Detailed Description
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Statement Reference Atg2[EP3697]/Df(3L)BSC119 mutants display basal autophagy defects in larval fat body cells. Atg2[EP3697] heterozygous neuromuscular junctions exhibit wild-type bouton levels. Atg2[EP3697]/Df(3L)Exel6091 animals analysed at +4 hours relative to puparium formation show a significant delay in midgut histolysis compared to controls. At +12 hours relative to puparium formation, larval midgut contraction is dramatically delayed in the mutants compared to controls. Atg2[EP3697] mutants exhibit neuromuscular junction undergrowth but do not exhibit defects in axonal transport. Mutants show disruption of autophagy. Mutant larvae expressing Atg2EP3697 under the control of Scer\GAL4elav-C155 have reduced or abnormal synapses. Mutant larvae expressing Atg2EP3697 under the control of Scer\GAL4elav-C155 have ISN neuron pathfinding defects. | |||
External Data
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| Linkouts | |||
Interactions
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Phenotypic Class
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Enhancer of | |||
Statement Reference | |||
Suppressor of | |||
Statement Reference Atg2EP3697, Scer\GAL4GMR.PF/Scer\GAL4GMR.PF is a suppressor of visible phenotype of Scer\GAL4GMR.PF/Scer\GAL4GMR.PF, bchsEP2299 | |||
Phenotype Manifest In
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Enhancer of | |||
Statement Reference | |||
Suppressor of | |||
Statement Reference Atg2EP3697, Scer\GAL4GMR.PF/Scer\GAL4GMR.PF is a suppressor of eye phenotype of Scer\GAL4GMR.PF/Scer\GAL4GMR.PF, bchsEP2299 | |||
Additional Comments
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Genetic Interactions
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Statement Reference An Atg2[EP3697] heterozygous background dominantly suppresses the increase in bouton number seen in Rae1[EX28] homozygous mutant neuromuscular junction. The modest neuromuscular undergrowth seen upon expression of hiw[Scer\UAS.fl] under the control of Scer\GAL4[elav-C155] is enhanced in a Atg2[EP3697] heterozygous background. | |||
Xenogenetic Interactions
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Statement Reference | |||
Complementation & Rescue Data
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| Comments | |||
Stocks
( 1 ) | |||
| Bloomington | |||
Notes on Origin
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| Discoverer | |||
External Crossreferences & Linkouts
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| Other Crossreferences | |||
| Linkouts | |||
Synonyms & Secondary IDs
( 3 ) | |||
| Reported As | |||
| Symbol Synonym | Atg2EP3697 atg2EP3697 EP3697EP3697 | ||
| Name Synonym | |||
| Secondary FlyBase IDs | |||
References
( 8 ) | |||
| Research paper |
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| Supplementary material |
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| Personal communication to FlyBase |
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Recent Updates
External Crossreferences & Linkouts