Phenotype ontology term - FYPO:0002219 - normal chromosome disjunction at meiosis I
Term summary
- ID
- FYPO:0002219
- Name
- normal chromosome disjunction at meiosis I
- Ontology or CV name
- Phenotype
- Definition
- A cellular process phenotype in which homologous chromosome segregation, or disjunction, is normal (i.e. indistinguishable from wild type).
Annotation
Multi-locus phenotype
References:
Genes:
Genotypes:
Single locus phenotype
References:
Genes:
Genotypes:
- clr4delta/clr4delta
- par1delta/par1delta
- ppa2delta/ppa2delta
- rec11-10A(S10A,S22A,S34A,S43A,S150A,S439A,S496A,S880A,T60A,T70A aa)
- rec11-10D(S10D,S22D,S34D,S43D,S150D,S439D,S496D,S880D,T60D,T70D aa)
- rec11delta/rec11delta
- rec12-Y98F(aa)
- rec12delta
- rec12delta/rec12delta
- rec7delta
- rec8+(wild type)[Overexpression]/rec8+(wild type)[Overexpression]
- sgo1delta
- sgo1delta/sgo1delta
- spo4delta
- spo6delta
- swi6delta/swi6delta