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.
14 entries for 14 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 |
---|---|---|---|---|---|---|
chemical compound accumulation: abnormal | systematic mutation set | null Allele: cit2-Δ | S288C | alpha-amino acid | Details: Significantly altered free amino acid profile (X^2- test p < 0.01), showing 1 simultaneous amino acid change (Z-test, adjusted p < 0.01) | Mülleder M, et al. (2016) PMID:27693354 |
chemical compound accumulation: increased | systematic mutation set | null Allele: cit2-Δ | S288C | aspartate(1-) | Mülleder M, et al. (2016) PMID:27693354 | |
chronological lifespan: decreased | classical genetics | null Allele: cit2-Δ | S288C | Media: glucose, 2 % Details: significant reduction in the CLS of the null mutant relative to wt under non-restricted conditions | Kwon YY, et al. (2024) PMID:38717792 | |
competitive fitness: increased | competitive growth fitness profiling using complete deletion alleles | null Allele: cit2-Δ | S288C | Media: minimal medium Details: Relative fitness score: 1.019 | Breslow DK, et al. (2008) PMID:18622397 | |
heat sensitivity: decreased | systematic mutation set high throughput heat ramp cell death assay | null Allele: cit2-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 | |
innate thermotolerance: decreased | systematic mutation set | null Allele: cit2-Δ | S288C | Treatment: heat shock, 50 °C Details: acquired thermotolerance is unaffected | Gibney PA, et al. (2013) PMID:24167267 | |
invasive growth: increased | homozygous diploid, systematic mutation set | overexpression | Sigma1278b | Media: nitrogen-sufficient medium Details: agar invasion score: 0.94; enhanced pseudohyphal growth, based on elevated invasiveness | Shively CA, et al. (2013) PMID:23410832 | |
mitochondrial morphology: abnormal | classical genetics | null Allele: cit2-Δ | W303 | Details: percentage of cells with tubular mitochondria is reduced from ~63% in wt cells to 50% in the null mutant; further decreased to ~37% by overexpression of OLE1 | Alsayyah C, et al. (2024) PMID:38669296 | |
protein/peptide distribution: abnormal Reporter: Fum1p | classical genetics | null Allele: cit2-Δ | S288C | Details: cytosolic activity and protein levels of fumarase are decreased, although total cellular fumarase activity is elevated | Regev-Rudzki N, et al. (2009) PMID:19415796 | |
resistance to chemicals: decreased | heterozygous diploid, systematic mutation set | null Allele: cit2-Δ | S288C | 30 μg/mL gemfibrozil | Lum PY, et al. (2004) PMID:14718172 |
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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