CDC37
Gene Ontology Biological Process
Gene Ontology Molecular Function
HIR3
Gene Ontology Biological Process
Gene Ontology Molecular Function
Gene Ontology Cellular Component
- HIR complex [IDA, IPI]
- nucleus [IDA]
Synthetic Growth Defect
A genetic interaction is inferred when mutations in separate genes, each of which alone causes a minimal phenotype, result in a significant growth defect under a given condition when combined in the same cell.
Publication
Multiple kinases and system robustness: a link between Cdc37 and genome integrity.
We identified 38 genes as having a genetic interaction with a mutant form of the kinase specific chaperone, Cdc37, using a genome-wide synthetic screening approach. The identified genes included a sub-network of highly interacting genes enriched for functions in genome integrity and comprising multiple components of several discrete molecular machines. A network analysis approach related these machines to a small ... [more]
Throughput
- High Throughput
Ontology Terms
- phenotype: vegetative growth (APO:0000106)
Additional Notes
- A synthetic genetic array (SGA) analysis was carried out to identify genes interacting with a mutant form of the kinase specific chaperone CDC37 (cdc37-S14A).
Related interactions
| Interaction | Experimental Evidence Code | Dataset | Throughput | Score | Curated By | Notes |
|---|---|---|---|---|---|---|
| CDC37 HIR3 | 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 | -0.206 | BioGRID | 367541 | |
| CDC37 HIR3 | 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 | -0.2899 | BioGRID | 1968988 | |
| HIR3 CDC37 | 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 | -0.268 | BioGRID | 2052846 |
Curated By
- BioGRID