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.
53 entries for 17 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 |
|---|---|---|---|---|---|---|
| bud morphology: abnormal | systematic mutation set | null Allele: ubc13-Δ | S288C | Details: bud is abnormally elongated | Watanabe M, et al. (2009) PMID:19466415 | |
| chemical compound accumulation: increased | homozygous diploid | null Allele: ubc13-Δ | S288C | cobalt(2+) | Treatment: cobalt dichloride, 1 mM Details: cobalt sensitive null mutant accumulates cobalt after treatment with CoCl2 for 12 hrs | Zhao YY, et al. (2020) PMID:31904504 |
| chemical compound accumulation: increased | homozygous diploid | null Allele: ubc13-Δ | S288C | reactive oxygen species | Treatment: cobalt dichloride, 1 mM Details: increased intracellular accumulation of ROS in cells treated with CoCl2 for 12 hrs; possible defect in scavenging oxidative stress | Zhao YY, et al. (2020) PMID:31904504 |
| chemical compound excretion: increased | systematic mutation set | null Allele: ubc13-Δ | S288C | inositol | Media: synthetic medium lacking inositol and choline Details: Opi- phenotype; overproduction and excretion of inositol in the absence of inositol and choline | Hancock LC, et al. (2006) PMID:16582425 |
| colony sectoring: increased | heterozygous diploid, systematic mutation set | null Allele: ubc13-Δ | S288C | Assay: quantitative chromosome transmission fidelity (qCTF) assay Details: >1.5 fold increase in mini-chromosome loss relative to wt, indicative of chromosome instability (CIN) | Zhu J, et al. (2015) PMID:25823586 | |
| competitive fitness: increased | competitive growth fitness profiling using complete deletion alleles | null Allele: ubc13-Δ | S288C | Media: minimal medium Details: Relative fitness score: 1.007 | Breslow DK, et al. (2008) PMID:18622397 | |
| competitive fitness: increased | homozygous diploid, competitive growth | null Allele: ubc13-Δ | S288C | Treatment: conditions that mimic Phase I of a batch fermentation, equivalent to ~14 hours after inoculation of a batch fermentation | Novo M, et al. (2013) PMID:24040173 | |
| competitive fitness: increased | homozygous diploid, competitive growth | null Allele: ubc13-Δ | S288C | Treatment: conditions that mimic Phase II of a batch fermentation, equivalent to ~22 hours after inoculation of a batch fermentation | Novo M, et al. (2013) PMID:24040173 | |
| heat sensitivity: decreased | classical genetics | overexpression | S288C | Temperature: elevated temperature, 39 °C | Hiraishi H, et al. (2006) PMID:17090950 | |
| heat sensitivity: decreased | systematic mutation set high throughput heat ramp cell death assay | null Allele: ubc13-Δ | S288C | Temperature: elevated temperature Details: ramp temperature from ambient to 30 deg C immediately, hold 1 min at 30 deg C, ramp temperature from 30 deg C to 62 deg C over 20 min, return to ambient | Teng X, et al. (2011) PMID:21814286 |
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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