Phenotype ontology term - FYPO:0007157 - abnormal histone binding
Term summary
- ID
- FYPO:0007157
- Name
- abnormal histone binding
- Ontology or CV name
- Phenotype
- Definition
- A molecular function phenotype in which occurrence of histone binding by a gene product (usually a protein) in a mutant is abnormal. The affected gene product may be encoded by the mutated gene, or by a different gene.
Annotation
Single locus phenotype
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- asf1-33(A16T,L61P,E119K,L121P,N156S,E180G aa)
- djc9-(1-72)(73-255 Δaa)
- djc9-(160-255)-L215A/I219A(1-159,L215A,I219A aa)
- djc9-(160-255)-L234R/Y238R(1-159,L234R,Y238R aa)
- djc9-(169-255)(1-168 Δaa)
- djc9-(95-159)(1-94,160-255 Δaa)
- mcm2-1(D87G,D112G aa)
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