MPS3
Gene Ontology Biological Process
- chromatin silencing at telomere [IMP]
- establishment of mitotic sister chromatid cohesion [IMP]
- karyogamy [IMP]
- meiotic telomere clustering [IGI, IMP]
- mitotic sister chromatid cohesion [IMP]
- nuclear migration involved in conjugation with cellular fusion [IMP]
- spindle pole body duplication [IMP]
- synapsis [IGI, IMP]
- telomere tethering at nuclear periphery [IMP]
Gene Ontology Cellular Component
MPS1
Gene Ontology Biological Process
- mitotic spindle assembly checkpoint [IGI, IMP]
- protein autophosphorylation [IDA]
- protein localization to kinetochore [IGI]
- protein phosphorylation [IDA, IMP]
- regulation of attachment of spindle microtubules to kinetochore [IMP]
- sister chromatid biorientation [IMP]
- spindle assembly [IMP]
- spindle pole body duplication [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
Mps3p is a novel component of the yeast spindle pole body that interacts with the yeast centrin homologue Cdc31p.
Accurate duplication of the Saccharomyces cerevisiae spindle pole body (SPB) is required for formation of a bipolar mitotic spindle. We identified mutants in SPB assembly by screening a temperature-sensitive collection of yeast for defects in SPB incorporation of a fluorescently marked integral SPB component, Spc42p. One SPB assembly mutant contained a mutation in a previously uncharacterized open reading frame that ... [more]
Throughput
- Low Throughput
Ontology Terms
- phenotype: inviable (APO:0000112)
Related interactions
Interaction | Experimental Evidence Code | Dataset | Throughput | Score | Curated By | Notes |
---|---|---|---|---|---|---|
MPS3 MPS1 | 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. | Low | - | BioGRID | 157483 |
Curated By
- BioGRID