Allele Dmel\nerfin-1159
| General Information | |||
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| Symbol | Dmel\nerfin-1159 | Species | D. melanogaster |
| Name | FlyBase ID | FBal0175568 | |
| Feature type | allele | Associated gene | Dmel\nerfin-1 |
| Allele class | |||
| Mutagen | recombination, FLPase, SCEI endonuclease, ends-in gene targeting | ||
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 Two deletions remove a 1314bp and a 593bp segment that includes the minimal promoter and 5' transcribed leader sequence. | ||
| 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 | |||
External Data
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| Linkouts | |||
Interactions
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Phenotypic Class
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Suppressor of | |||
Statement Reference nerfin-1159/nerfin-1[+] is a suppressor | partially | somatic clone of neuroanatomy defective | somatic clone | adult stage phenotype of prosIG2227 | |||
Phenotype Manifest In
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Suppressor of | |||
Statement Reference nerfin-1159/nerfin-1[+] is a suppressor | partially | somatic clone of carbon dioxide sensitive neuron | ectopic | somatic clone phenotype of prosIG2227 | |||
Additional Comments
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Genetic Interactions
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Statement Reference The number of ectopic CO[[2]] neurons on the maxillary palp in animals containing pros[IG2227] clones is significantly suppressed if they are also carrying nerfin-1[159]/+. | |||
Xenogenetic Interactions
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Statement Reference | |||
Complementation & Rescue Data
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| Comments | |||
Stocks
( 0 ) | |||
Notes on Origin
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| Discoverer | |||
Comments
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Created as a consequence of the "ends in" homologous recombination gene knockout technique. The deletion was most likely caused by exonuclease digestion of the targeting vector after the SceI exonuclease induced double strand break but before its integration into the nerfin-1 chromosomal locus. The deletion was detected after the allelic substitution step and are most likely the result of illegitimate recombination between micro-homologies present in the minimal promoter of one copy of the nerfin-1 duplication and the transcribed region of the tandem copy. | |||
External Crossreferences & Linkouts
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| Other Crossreferences | |||
| Linkouts | |||
Synonyms & Secondary IDs
( 4 ) | |||
| Reported As | |||
| Symbol Synonym | Df(3L)nerfin-1159 nerfin-1159 nerfin-1null nerfin159 | ||
| Name Synonym | |||
| Secondary FlyBase IDs | |||
References
( 2 ) | |||
| Research paper |
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Recent Updates
External Crossreferences & Linkouts