Phenotype ontology term - FYPO:0006526 - abnormal meiosis II
Term summary
- ID
- FYPO:0006526
- Name
- abnormal meiosis II
- Ontology or CV name
- Phenotype
- Definition
- A cellular process phenotype in which the second meiotic nuclear division is abnormal.
Annotation
Multi-locus phenotype
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- bqt1delta klp6delta sad1.2(T3S,S52P aa)
- mes1delta slp1-NF410(unknown)
- mfr1delta slp1-NF410(unknown)
- rec11delta rec8-RDRD(D369R,D370R,R373E,E379R,E381R,R384E aa)
- rec11delta rec8-RDRD(D369R,D370R,R373E,E379R,E381R,R384E aa) sgo1delta
- rec11delta rec8-RDRD(D369R,D370R,R373E,E379R,E381R,R384E aa) sgo2delta
- rec8-RDRD(D369R,D370R,R373E,E379R,E381R,R384E aa) sgo1delta
- rec8-RDRD(D369R,D370R,R373E,E379R,E381R,R384E aa) sgo2delta
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Single locus phenotype
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- cdc13+(wild type)[Knockdown]
- cdc13-117(C379Y aa)
- cdc2-33(A177T aa)
- cdc2-7(unknown)
- cdc25-22(C532Y aa)
- mes1-K0(K7R,K16R,K46R,K54R,K86R,K57R,K58R,K90R,K55R aa)
- mes1delta
- rec8-RDRD(D369R,D370R,R373E,E379R,E381R,R384E aa)
- slp1-NF410(unknown)
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