Phenotype ontology term - FYPO:0003633 - abolished U1 snRNP binding

Term summary

ID

FYPO:0003633

Name

abolished U1 snRNP binding

Ontology or CV name

Phenotype

Definition

A molecular function phenotype in which U1 snRNP binding by a gene product does not occur. The affected gene product may be encoded by the mutated gene, or by a different gene.

Parents

• is_a abolished protein-protein interaction
• is_a abnormal ribonucleoprotein complex binding

Annotation