Phenotype Help

SHE1 / YBL031W 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.

53 entries for 27 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
anaerobic growth: decreased
systematic mutation setnull
Allele: she1-Δ
S288CDetails: anaerobic growth on media supplemented with either ergosterol or cholesterol is reduced
Reiner S, et al. (2006) PMID:16251356
biofilm formation: decreased
systematic mutation setnull
Allele: she1-Δ
S288CVandenbosch D, et al. (2013) PMID:24034557
budding index: abnormal
classical geneticsoverexpressionS288CSopko R, et al. (2006) PMID:16455487
budding index: decreased
classical geneticsoverexpressionOtherDetails: G1 arrested cells considerably larger than control cells
Espinet C, et al. (1995) PMID:7762298
cell cycle progression in G2 phase: abnormal
classical geneticsoverexpressionS288CDetails: see Table S8 for more details; shift towards 2C DNA content
Sopko R, et al. (2006) PMID:16455487
cell cycle progression: abnormal
systematic mutation setoverexpressionS288CDetails: accumulation of cells with a 2C DNA content and an increased percentage of large-budded cells indicative of a G2 or M phase delay or arrest
Niu W, et al. (2008) PMID:18617996
cell size: increased
classical geneticsoverexpressionS288CDetails: see Table S7 for more details
Sopko R, et al. (2006) PMID:16455487
chromosome/plasmid maintenance: decreased
heterozygous diploid, systematic mutation set overexpressionS288CDetails: mean frequency of loss of heterozygosity (LOH) at the CAN1 locus increased at least 2-fold; frequently accompanied by LOH at the MET6 locus indicating loss of the entire chr V
Tutaj H, et al. (2019) PMID:30244280
competitive fitness: decreased
systematic mutation set

fitness profiling after 15 generations

null
Allele: she1-Δ
S288CMedia: alkaline conditions, pH 8
Giaever G, et al. (2002) PMID:12140549
competitive fitness: decreased
competitive growth

fitness profiling using complete deletion alleles

null
Allele: she1-Δ
S288CMedia: minimal medium
Details: Relative fitness score: 0.907
Breslow DK, et al. (2008) PMID:18622397
Showing 1 to 10 of 53 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).


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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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