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General Information
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| Term |
amorphic allele - genetic evidence |
ID (Ontology) |
FBcv:0000288 (FlyBase CV) |
| Definition |
An allele inferred to completely lack function from the observation that addition of extra copies in the genome has no effect on the phenotype. Most commonly, evidence takes the form of the observation that the phenotype of homozygotes (2 copies) is identical to that seen when the allele is in trans to a deletion of the gene (1 copy).[ FlyBase:FBrf0002371 FlyBase:FBrf0049147 ] |
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Links to External 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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| Alleles (FBal) | ALLELE_CLASS | 2012 | | Alleles (FBal) | PROMOTED_CLASS | 1694 |
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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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| Alleles |
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amorphic allele - genetic evidence (all annotations which use CV term, excluding "NOT" statements) | 2012 |
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