Phenotype ontology term - FYPO:0001093 - abolished chromatin binding

Term summary

ID

FYPO:0001093

Name

abolished chromatin binding

Ontology or CV name

Phenotype

Definition

A molecular function phenotype in which chromatin 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, and may normally bind DNA, protein, or both in chromatin.

Parents

• is_a abnormal chromatin binding

Annotation