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Phenotype ontology term - FYPO:0007250 - abnormal lipid binding

Term summary

ID
FYPO:0007250
Name
abnormal lipid binding
Ontology or CV name
Phenotype
Definition
A molecular function phenotype in which occurrence of lipid binding by a gene product (usually a protein) in a mutant is abnormal. The affected gene product may be encoded by the mutated gene, or by a different gene.

Parents

Annotation

Single locus phenotype

FYPO:0006937 - abolished lipid binding

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FYPO:0007253 - abolished membrane lipid binding

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FYPO:0007252 - decreased membrane lipid binding

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