Phenotype ontology term - FYPO:0002786 - decreased riboflavin binding

Term summary

ID

FYPO:0002786

Name

decreased riboflavin binding

Ontology or CV name

Phenotype

Definition

A molecular function phenotype in which occurrence of riboflavin binding by a gene product (usually a protein) in a mutant is decreased. The affected gene product may be encoded by the mutated gene, or by a different gene.

Parents

• is_a abnormal riboflavin binding

Annotation