Phenotype Help

SIP3 / YNL257C 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.

45 entries for 15 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
apoptosis: decreased
classical genetics null
Allele: sip3-Δ
W30360 μM amiodaroneDetails: decreased sensitivity to amiodarone-induced regulated cell death; survival increased from 5% in wt cells to 18% in the null mutant
Sokolov SS, et al. (2020) PMID:32564734
chemical compound accumulation: increased
classical genetics null
Allele: sip3-Δ
S288C ethanolTreatment: vanillin, 7 mM
Details: increased production of ethanol by the null mutant (8.6 g/l) at 24 hours relative to wt (3.6 g/l) in vanillin treated cells
Zhao F, et al. (2023) PMID:36528179
chromosome/plasmid maintenance: abnormal
large-scale survey

assay for maintenance of 5ORIdelta-deltaR fragment (derivative of Chromosome III lacking all efficient origins)

null
Allele: sip3-Δ
S288CDetails: originless fragment maintenance (Ofm) phenotype
Theis JF, et al. (2010) PMID:21151954
competitive fitness: decreased
systematic mutation set

fitness profiling after 15 generations

null
Allele: sip3-Δ
S288C10 uM nystatinGiaever G, et al. (2002) PMID:12140549
competitive fitness: decreased
systematic mutation set

fitness profiling after 5 generations

null
Allele: sip3-Δ
S288C10 uM nystatinGiaever G, et al. (2002) PMID:12140549
competitive fitness: increased
competitive growth

fitness profiling using complete deletion alleles

null
Allele: sip3-Δ
S288CMedia: minimal medium
Details: Relative fitness score: 1.004
Breslow DK, et al. (2008) PMID:18622397
competitive fitness: increased
systematic mutation setnull
Allele: sip3-Δ
S288CMedia: synthetic complete medium, SC
Qian W, et al. (2012) PMID:23103169
desiccation resistance: decreased
homozygous diploid, systematic mutation setnull
Allele: sip3-Δ
S288CTreatment: pooled mutants subject to three cycles of growth to post-diauxic phase followed by desiccation and regrowth
Details: 2-fold or greater decreased survival after the treatment
Ratnakumar S, et al. (2011) PMID:20963216
growth in exponential phase: increased rate
classical genetics null
Allele: sip3-Δ
S288C7 mM vanillinDetails: shorter lag phase and better growth on vanillin-containing media with a fermentable carbon source relative to wt
Zhao F, et al. (2023) PMID:36528179
heat sensitivity: increased
systematic mutation setnull
Allele: sip3-Δ
S288CTemperature: elevated temperature, 39 °C
Details: medium heat-sensitivity
Ruiz-Roig C, et al. (2010) PMID:20398213
Showing 1 to 10 of 45 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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