Phenotype ontology term - FYPO:0003636 - decreased U2 snRNP binding

Term summary

ID

FYPO:0003636

Name

decreased U2 snRNP binding

Ontology or CV name

Phenotype

Definition

A molecular function phenotype in which U2 snRNP binding by a gene product is decreased. The affected gene product may be encoded by the mutated gene, or by a different gene.

Parents

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

Annotation