Phenotype Help

RSB1 / YOR049C Phenotype

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.



Annotations

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 8 phenotypes


Increase 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.

PhenotypeExperiment TypeMutant InformationStrain BackgroundChemicalDetailsReference
chemical compound accumulation: increased
classical genetics overexpressionS288C sphingolipidTreatment: myriocin, 0.07 μg/ml
Details: increased levels of complex sphingolipids in myriocin-treated cells where levels are reduced
Kawaguchi T, et al. (2024) PMID:39104838
competitive fitness: increased
competitive growth

fitness profiling using complete deletion alleles

null
Allele: rsb1-Δ
S288CMedia: minimal medium
Details: Relative fitness score: 1.001
Breslow DK, et al. (2008) PMID:18622397
competitive fitness: increased
systematic mutation setnull
Allele: rsb1-Δ
S288C ethanolQian W, et al. (2012) PMID:23103169
competitive fitness: increased
systematic mutation setnull
Allele: rsb1-Δ
S288CMedia: glycerol medium, YPG
Qian W, et al. (2012) PMID:23103169
competitive fitness: increased
systematic mutation setnull
Allele: rsb1-Δ
S288CMedia: rich medium (YPD) w/6% ethanol, ETH
Qian W, et al. (2012) PMID:23103169
heat sensitivity: decreased
systematic mutation set

high throughput heat ramp cell death assay

null
Allele: rsb1-Δ
S288CTemperature: 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
invasive growth: increased
homozygous diploid, systematic mutation setoverexpressionSigma1278bMedia: nitrogen-sufficient medium
Details: agar invasion score: 0.94; enhanced pseudohyphal growth, based on elevated invasiveness
Shively CA, et al. (2013) PMID:23410832
resistance to chemicals: decreased
classical geneticsnull
Allele: rsb1-Δ
SEY621010 uM phytosphingosinePanwar SL and Moye-Rowley WS (2006) PMID:16407254
resistance to chemicals: decreased
competitive growth

fitness profiling of the non-essential deletion collection after 18 generations

null
Allele: rsb1-Δ
S288C20 ug/ml cordycepinDetails: sensitivity increased two-fold or greater
Holbein S, et al. (2009) PMID:19324962
resistance to chemicals: decreased
heterozygous diploid, systematic mutation set null
Allele: rsb1-Δ
S288C2.5 mg/mL procaineLum PY, et al. (2004) PMID:14718172
Showing 1 to 10 of 14 entries

Shared Phenotypes

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).


Reset

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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