Phenotype ontology term - FYPO:0003891 - normal intragenic meiotic recombination
Term summary
- ID
- FYPO:0003891
- Name
- normal intragenic meiotic recombination
- Ontology or CV name
- Phenotype
- Definition
- A cellular process phenotype in which the occurrence of intragenic meiotic recombination is normal (i.e. indistinguishable from wild type). Intragenic meiotic recombination can result in gene conversion events.
Annotation
Single locus phenotype
References:
Genes:
Genotypes:
- ade6-M375(G45*)
- fml1delta
- mek1-T15A(aa)
- mek1-T318A(aa)
- mek1-T322A(aa)
- rad52delta
- rec10-cdk-total(S347A,T410A,T482A,S529A,T532A,T566A,T638A,S651A aa)
- rec14-cdk-site2(S188A aa)
- rec27-242(K52E aa)
- rec27-243(K57E aa)
- rec27-244(K65E aa)
- rec27-245(K108E aa)
- rec27-cdk(T115A aa)
- rec7-cdk-site1,2(T243A,S244A,S245A,T268A aa)
- rec7-cdk-site1(T243A,S244A,S245A aa)
- rec7-cdk-site2(T268A aa)
- rec8-S412A(aa)
- sfr1-7A (CDK sites)(T73A,T89A,S109A,S116A,S147A,T152A,S165A aa)/sfr1-7A (CDK sites)(T73A,T89A,S109A,S116A,S147A,T152A,S165A aa)
- tsn1delta
