General Information
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Term |
phiC31 integrase |
ID (Ontology) |
FBcv:0003010 (FlyBase CV) |
Definition |
Sequence change caused by a site specific recombination catalyzed by the serine recombinase phiC31 integrase that recognizes a minimal high-efficiency attP recognition site of 39 base pairs and a minimal high-efficiency attB recognition site of 34 base pairs. The attP and attB sites contain imperfect inverted repeats flanking a short recombination core (TTG) that provides directionality.[ FlyBase:FBrf0174693 FlyBase:FBrf0201927 ] |
Also Known As |
"change induced by phiC31 integrase recombination" |
Comment |
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Links to Extrernal Ontologies
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Annotations
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Records annotated with this term OR any of its CHILD TERMS
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Records annotated with this exact term (annotations to child terms are NOT included)
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Data Class | Field | Records |
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Aberrations (FBab) | MUTAGEN | 1028 | Alleles (FBal) | MUTAGEN | 4241 |
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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Full annotation statements | Relevant FlyBase reports |
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Aberrations | Alleles |
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phiC31 integrase (all annotations which use CV term, excluding "NOT" statements) | 1028 | 4241 |
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