Phenotype ontology term - FYPO:0002980 - increased chromatin binding

Term summary

ID

FYPO:0002980

Name

increased chromatin binding

Ontology or CV name

Phenotype

Definition

A molecular function phenotype in which occurrence of chromatin binding by a gene product (usually a protein) in a mutant is increased. 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