VPS21
Gene Ontology Biological Process
Gene Ontology Molecular Function
Gene Ontology Cellular Component
MON2
Gene Ontology Biological Process
Gene Ontology Molecular Function
Gene Ontology Cellular Component
Synthetic Lethality
A genetic interaction is inferred when mutations or deletions in separate genes, each of which alone causes a minimal phenotype, result in lethality when combined in the same cell under a given condition.
Publication
Use of a synthetic lethal screen to identify yeast mutants impaired in endocytosis, vacuolar protein sorting and the organization of the cytoskeleton.
To identify new genes whose products act on the endocytic and vacuolar protein sorting pathways, we screened for mutants that display synthetic growth defects with delta ypt51, a mutant impaired in membrane traffic at a point where these pathways intersect. Seven mutants that fell into six different complementation groups were found to fit this criterium. Two of the mutants (ysl1 ... [more]
Throughput
- Low Throughput
Ontology Terms
- phenotype: inviable (APO:0000112)
Related interactions
Interaction | Experimental Evidence Code | Dataset | Throughput | Score | Curated By | Notes |
---|---|---|---|---|---|---|
MON2 VPS21 | Positive Genetic Positive Genetic Mutations/deletions in separate genes, each of which alone causes a minimal phenotype, but when combined in the same cell results in a less severe fitness defect than expected under a given condition. This term is reserved for high or low throughput studies with scores. | High | 3.1508 | BioGRID | 514418 | |
MON2 VPS21 | Positive Genetic Positive Genetic Mutations/deletions in separate genes, each of which alone causes a minimal phenotype, but when combined in the same cell results in a less severe fitness defect than expected under a given condition. This term is reserved for high or low throughput studies with scores. | High | 3.0338 | BioGRID | 209496 | |
VPS21 MON2 | Positive Genetic Positive Genetic Mutations/deletions in separate genes, each of which alone causes a minimal phenotype, but when combined in the same cell results in a less severe fitness defect than expected under a given condition. This term is reserved for high or low throughput studies with scores. | High | 3.0338 | BioGRID | 212360 |
Curated By
- BioGRID