Phenotype annotations for a gene are curated single mutant phenotypes that require an observable (e.g., "cell shape"), a qualifier (e.g., "abnormal"), a mutant type (e.g., null), strain background, and a reference. In addition, annotations are classified as classical genetics or high-throughput (e.g., large scale survey, systematic mutation set). Whenever possible, allele information and additional details are provided.
A phenotype is defined as an observable (e.g., apoptosis) and a qualifier (e.g., increased). There may be more than one row with the same phenotype if that phenotype was observed in separate studies or in different conditions, strains, alleles, etc.
20 entries for 12 phenotypesIncrease the total number of rows showing on this page using the pull-down located below the table, or use the page scroll at the table's top right to browse through the table's pages; use the arrows to the right of a column header to sort by that column; filter the table using the "Filter" box at the top of the table; click on the small "i" buttons located within a cell for an annotation to view further details.
| Phenotype | Experiment Type | Mutant Information | Strain Background | Chemical | Details | Reference |
|---|---|---|---|---|---|---|
| chromosome segregation: abnormal | classical genetics | conditional Allele: spc24-1 | Other | Temperature: elevated temperature, 36 °C Details: centromeres fail to split during spindle elongation, some centromeres detach from spindle | Wigge PA and Kilmartin JV (2001) PMID:11266451 | |
| chromosome segregation: abnormal | classical genetics | conditional Allele: spc24-11 S109P, K171N | S288C | Temperature: elevated temperature, 37 °C Details: assemble and elongate spindle in absence of chromosome segregation; defect not detected by mitotic checkpoint pathways | Le Masson I, et al. (2002) PMID:11952896 | |
| chromosome/plasmid maintenance: decreased | large-scale survey | repressible | S288C | 10 ug/ml doxycycline | Details: Tet-regulated essential ORF strain collection (doxycycline represses expression)|; increased chromosome rearrangements and chromosome loss, as measured in an illegitimate mating assay | Cheng E, et al. (2012) PMID:22673806 |
| colony sectoring: increased | large-scale survey | conditional Allele: spc24-10 | S288C | Assay: chromosome transmission fidelity (CTF) assay Temperature: semi-permissive temperature Details: indicative of chromosome instability (CIN); metascore strong (single hit) | Stirling PC, et al. (2011) PMID:21552543 | |
| competitive fitness: decreased | competitive growth fitness profiling of essential genes using hypomorphic DAmP alleles | reduction of function | S288C | Media: minimal medium Details: Relative fitness score: 0.989 | Breslow DK, et al. (2008) PMID:18622397 | |
| haploproficient | heterozygous diploid, competitive growth genome-wide fitness profiling | null Allele: spc24-Δ | S288C | Media: turbidostat growth in FPM medium Details: Relative growth score: 0.0088 | Pir P, et al. (2012) PMID:22244311 | |
| heat sensitivity: increased | classical genetics | conditional Allele: spc24-2 | Other | Temperature: elevated temperature, 33 °C | Janke C, et al. (2001) PMID:11179222 | |
| heat sensitivity: increased | classical genetics | conditional Allele: spc24-11 S109P, K171N | S288C | Temperature: elevated temperature, 37 °C | Le Masson I, et al. (2002) PMID:11952896 | |
| heat sensitivity: increased | classical genetics | conditional Allele: spc24-9 | S288C | Temperature: elevated temperature, 33 °C | Ma L, et al. (2012) PMID:22870406 | |
| innate thermotolerance: decreased | homozygous diploid, systematic mutation set | null Allele: spc24-Δ | S288C | Phase: exponential phase Treatment: heat shock, 50 °C Details: sensitivity scale of -1 (least) to -4 (most) sensitive: -1 | Jarolim S, et al. (2013) PMID:24142923 |
This diagram displays phenotype observables (purple squares) that are shared between the given gene (yellow circle) and other genes (gray circles) based on the number of phenotype observables shared (adjustable using the slider at the bottom).
Click on a gene or phenotype observable name to go to its specific page within SGD; drag any of the gene or observable objects around within the visualization for easier viewing; click “Reset” to automatically redraw the diagram; filter the genes that share observable terms with the given gene by the number of terms they share by clicking anywhere on the slider bar or dragging the tab to the desired filter number.
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