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General Information
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| Term |
hypomorphic allele - genetic evidence |
ID (Ontology) |
FBcv:0000289 (FlyBase CV) |
| Definition |
Allele inferred to make a gene product that is functionally equivalent to wild-type but in a lesser amount or with lowered activity from the observation that extra copies in the genome decrease the expressivity and/or penetrance of the phenotype. Most commonly this evidence takes the form of experiments showing that the homozygote (2 copies) has a weaker phenotype than the allele 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 | 2314 | | Alleles (FBal) | PROMOTED_CLASS | 2138 |
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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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hypomorphic allele - genetic evidence (all annotations which use CV term, excluding "NOT" statements) | 2314 |
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