CDC11
Gene Ontology Biological Process
Gene Ontology Molecular Function
Gene Ontology Cellular Component
SWE1
Gene Ontology Biological Process
- G2 cell size control checkpoint [IEP, IMP]
- G2/M transition of mitotic cell cycle [IDA, IMP, ISS]
- cytokinesis after mitosis checkpoint [IDA, IEP, IMP]
- negative regulation of spindle pole body separation [IGI, IMP]
- protein phosphorylation [IDA]
- re-entry into mitotic cell cycle [IGI]
- regulation of cell size [IMP]
- regulation of cyclin-dependent protein serine/threonine kinase activity [IDA]
- regulation of meiosis [IEP, IGI, IMP]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
Phenotypic Suppression
A genetic interaction is inferred when mutation or over expression of one gene results in suppression of any phenotype (other than lethality/growth defect) associated with mutation or over expression of another gene.
Publication
Septin-dependent assembly of a cell cycle-regulatory module in Saccharomyces cerevisiae.
Saccharomyces cerevisiae septin mutants have pleiotropic defects, which include the formation of abnormally elongated buds. This bud morphology results at least in part from a cell cycle delay imposed by the Cdc28p-inhibitory kinase Swe1p. Mutations in three other genes (GIN4, encoding a kinase related to the Schizosaccharomyces pombe mitotic inducer Nim1p; CLA4, encoding a p21-activated kinase; and NAP1, encoding a ... [more]
Throughput
- Low Throughput
Ontology Terms
- bud morphology (APO:0000212)
Related interactions
Interaction | Experimental Evidence Code | Dataset | Throughput | Score | Curated By | Notes |
---|---|---|---|---|---|---|
CDC11 SWE1 | Negative Genetic Negative Genetic Mutations/deletions in separate genes, each of which alone causes a minimal phenotype, but when combined in the same cell results in a more severe fitness defect or lethality under a given condition. This term is reserved for high or low throughput studies with scores. | High | -0.1493 | BioGRID | 392501 | |
CDC11 SWE1 | Negative Genetic Negative Genetic Mutations/deletions in separate genes, each of which alone causes a minimal phenotype, but when combined in the same cell results in a more severe fitness defect or lethality under a given condition. This term is reserved for high or low throughput studies with scores. | High | -0.149 | BioGRID | 911525 |
Curated By
- BioGRID