POL1
Gene Ontology Biological Process
- DNA replication [IMP]
- DNA replication checkpoint [IBA]
- DNA replication initiation [IC]
- DNA replication, synthesis of RNA primer [IBA]
- DNA strand elongation involved in DNA replication [IBA]
- DNA synthesis involved in DNA repair [IMP]
- RNA-dependent DNA replication [IDA]
- double-strand break repair [IMP]
- gene conversion at mating-type locus, DNA repair synthesis [IBA]
- lagging strand elongation [IC]
- premeiotic DNA replication [IMP]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
RAD24
Gene Ontology Biological Process
Gene Ontology Molecular Function
Gene Ontology Cellular Component
Dosage Lethality
A genetic interaction is inferred when over expression or increased dosage of one gene causes lethality in a strain that is mutated or deleted for another gene.
Publication
G2/M checkpoint genes of Saccharomyces cerevisiae: further evidence for roles in DNA replication and/or repair.
We have cloned, sequenced and disrupted the checkpoint genes RAD17, RAD24 and MEC3 of Saccharomyces cerevisiae. Mec3p shows no strong similarity to other proteins currently in the database. Rad17p is similar to Rec1 from Ustilago maydis, a 3' to 5' DNA exonuclease/checkpoint protein, and the checkpoint protein Rad1p from Schizosaccharomyces pombe (as we previously reported). Rad24p shows sequence similarity to ... [more]
Throughput
- Low Throughput
Ontology Terms
- phenotype: inviable (APO:0000112)
Related interactions
Interaction | Experimental Evidence Code | Dataset | Throughput | Score | Curated By | Notes |
---|---|---|---|---|---|---|
POL1 RAD24 | 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 | -0.1824 | BioGRID | 2008941 | |
POL1 RAD24 | 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 | 1518459 |
Curated By
- BioGRID