Phenotype Help

VTC3 / YPL019C 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.

19 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
biofilm formation: decreased
systematic mutation setnull
Allele: vtc3-Δ
Sigma1278bScherz K, et al. (2014) PMID:25009170
chemical compound accumulation: decreased
classical geneticsnull
Allele: vtc3-Δ
Other polyphosphateTreatment: polyphosphate overplus (phosphate starvation followed by high phosphate treatment)
Details: significant reduction in polyphosphate levels (14% of wildtype)
Ogawa N, et al. (2000) PMID:11102525
chemical compound accumulation: decreased
classical geneticsreduction of function
Allele: vtc3- K130A/K133A

within SPX domain

S288C polyphosphateWild R, et al. (2016) PMID:27080106
chemical compound accumulation: decreased
classical geneticsreduction of function
Allele: vtc3- K133A/K136A

within SPX domain

S288C polyphosphateWild R, et al. (2016) PMID:27080106
chitin deposition: increased
systematic mutation set null
Allele: vtc3-Δ
S288CDetails: increased cell wall chitin using a five cycle reiterative enrichment strategy and FACS sorting of cells labelled with either GFP-tagged chitinase or Calcofluor white
Chuene LT, et al. (2024) PMID:39270658
chitin deposition: increased
classical genetics null
Allele: vtc3-Δ
S288CDetails: increased cell wall chitin using both flow cytometry with Calcofluor white staining and GFP chitinase
Chuene LT, et al. (2024) PMID:39270658
colony appearance: abnormal
systematic mutation setnull
Allele: vtc3-Δ
Sigma1278bMedia: YP sucrose plates
Details: little bit wrinkly in the middle compared to the overall wrinkled appearance of wt colonies
Voordeckers K, et al. (2012) PMID:22882838
competitive fitness: increased
competitive growth

fitness profiling using complete deletion alleles

null
Allele: vtc3-Δ
S288CMedia: minimal medium
Details: Relative fitness score: 1.011
Breslow DK, et al. (2008) PMID:18622397
metal resistance: decreased
systematic mutation set overexpressionS288C20 mM manganese(II) chlorideDetails: exacerbates toxicity
Chakrabortee S, et al. (2016) PMID:27693355
metal resistance: increased
systematic mutation setnull
Allele: vtc3-Δ
S288C25 mM manganese(2+)Chesi A, et al. (2012) PMID:22457822
Showing 1 to 10 of 19 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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