Phenotype ontology term - FYPO:0006799 - abolished nuclear MIS12/MIND complex binding
Term summary
- ID
- FYPO:0006799
- Name
- abolished nuclear MIS12/MIND complex binding
- Ontology or CV name
- Phenotype
- Definition
- A molecular function phenotype in which nuclear MIS12/MIND complex 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.
Annotation
Single locus phenotype
References:
Genes:
Genotypes:
- cnp3-26-49(1-25,50-643 Δaa)
- cnp3-26-52-E44A(1-25,53-643,E44A aa)
- cnp3-26-52-F30A(1-25,53-643,F30A aa)
- cnp3-26-52-F43A(1-25,53-643,F43A aa)
- cnp3-26-52-F50A(1-25,53-643,F50A aa)
- cnp3-26-52-K27A(1-25,53-643,K27A aa)
- cnp3-26-52-K38A(1-25,53-643,K38A aa)
- cnp3-26-52-R26A(1-25,53-643,R26A aa)
- cnp3-26-52-Y49A(1-25,53-643,Y49A aa)
- cnp3-27-49(1-26,50-643 Δaa)
- cnp3-27-50(1-26,51-643 Δaa)
