Phenotype Help

YOR121C 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.

7 entries for 7 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
competitive fitness: decreased
competitive growth

fitness profiling using complete deletion alleles

null
Allele: yor121c-Δ
S288CMedia: minimal medium
Details: Relative fitness score: 0.996
Breslow DK, et al. (2008) PMID:18622397
filamentous growth: increased
systematic mutation setoverexpressionSigma1278bJin R, et al. (2008) PMID:17989363
haploinsufficient
heterozygous diploid, competitive growth

genome-wide fitness profiling

null
Allele: yor121c-Δ
S288CMedia: turbidostat growth in FPM medium
Details: Relative growth score: -0.0032
Pir P, et al. (2012) PMID:22244311
resistance to chemicals: decreased
heterozygous diploid, systematic mutation set null
Allele: yor121c-Δ
S288C20 μg/mL actinomycin DLum PY, et al. (2004) PMID:14718172
silencing: decreased
classical genetics null
Allele: yor121c-Δ
S288CDetails: decreased silencing at the silent mating type locus HMR based on expression of integrated URA3 using conventional spot tests
Liu Q, et al. (2020) PMID:32469861
vacuolar morphology: abnormal
systematic mutation set

screen all non-essential genes for inability to fragment vacuoles in response to salt addition

null
Allele: yor121c-Δ
S288C0.4 M sodium chlorideDetails: small defect in vacuolar fragmentation
Michaillat L and Mayer A (2013) PMID:23383298
viable
systematic mutation setnull
Allele: yor121c-Δ
S288CGiaever G, et al. (2002) PMID:12140549
Showing 1 to 7 of 7 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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