Phenotype ontology term - FYPO:0001839 - normal minichromosome loss
Term summary
- ID
- FYPO:0001839
- Name
- normal minichromosome loss
- Ontology or CV name
- Phenotype
- Definition
- A cell phenotype in which minichromosomes are lost at the same frequency as in wild-type cells. Minichromosome loss occurs when one or both daughter cells do not inherit copies of a minichromosome from the mother cell, and may result from failure of minichromosome replication or segregation.
Annotation
Multi-locus phenotype
References:
Genes:
Genotypes:
Single locus phenotype
References:
Genes:
Genotypes:
- abo2delta
- bub3delta
- cdc27-P11(G57E aa)
- chp2delta(139-380)(aa)
- clr1-5(unknown)
- clr2-E22(unknown)
- dfp1-3A(P448A,V450A,I452A aa)
- dis1-S551A,S556A,S590A(aa)
- dis1-T279A,S293A,S300A(aa)
- git7-235(A69E aa)
- grt1delta
- hat1delta
- hos2delta
- ima1delta
- leo1::Hermes(disruption)
- ned1-G80A(aa)
- pab1::ura4+
- pmt1delta
- psm3-K105N,K106N(aa)
- psm3-K105R(aa)
- rad55delta/rad55delta
- rap1-7A(S317A,S329A,S484A,S487A,S496A,S497A,S538A aa)
- rap1-7E(S317E,S329E,S484E,S487E,S496E,S497E,S538E aa)
- rec8-Asp-Cter(M1D,2-384 aa)
- sfh1-7(E142G,D329E,K393R aa)
- sfr1delta/sfr1delta
- sld3-5A(T636A,T650A,S673A,T690A,S698A aa)
- sld3-9A(S140A,T201A,T228A,S499A,T636A,T650A,S673A,T690A,S698A aa)
- spc7-9TE(T257E,T338E,T366E,T395E,T422E,T453E,T507E,T529E,T552E aa)
- wpl1delta
