Phenotype ontology term - FYPO:0002785 - abolished riboflavin binding

Term summary

ID

FYPO:0002785

Name

abolished riboflavin binding

Ontology or CV name

Phenotype

Definition

A molecular function phenotype in which riboflavin binding by a gene product (usually a protein) in a mutant does not occur. The affected gene product may be encoded by the mutated gene, or by a different gene.

Parents

• is_a abnormal riboflavin binding

Annotation