NBP2
Gene Ontology Biological Process
RTG2
Gene Ontology Biological Process
- maintenance of DNA trinucleotide repeats [IMP]
- mitochondria-nucleus signaling pathway [IMP]
- negative regulation of extrachromosomal rDNA circle accumulation involved in replicative cell aging [IMP]
- nitrogen catabolite regulation of transcription from RNA polymerase II promoter [IMP]
- positive regulation of transcription from RNA polymerase II promoter [IDA, IGI, IMP]
- regulation of transcription from RNA polymerase II promoter [IMP]
- transcription factor import into nucleus [IMP]
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
Systematic genetic analysis with ordered arrays of yeast deletion mutants.
In Saccharomyces cerevisiae, more than 80% of the approximately 6200 predicted genes are nonessential, implying that the genome is buffered from the phenotypic consequences of genetic perturbation. To evaluate function, we developed a method for systematic construction of double mutants, termed synthetic genetic array (SGA) analysis, in which a query mutation is crossed to an array of approximately 4700 deletion ... [more]
Throughput
- High Throughput
Ontology Terms
- inviable (APO:0000112)
Related interactions
Interaction | Experimental Evidence Code | Dataset | Throughput | Score | Curated By | Notes |
---|---|---|---|---|---|---|
NBP2 RTG2 | 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 | -5.22 | BioGRID | 2358775 | |
NBP2 RTG2 | 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 | 0.1686 | BioGRID | 2435025 | |
NBP2 RTG2 | Synthetic Growth Defect 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. | High | - | BioGRID | 450365 |
Curated By
- BioGRID