Phenotype Help

TAZ1 / YPR140W 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.


Summary
Non-essential gene; null mutants are subject to chromosome instability, sensitive to osmotic stress and starvation, have abnormal mitochondria and are impaired in respiration; overexpression enhances pseudohyphal growth in strain Sigma1278b

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.

36 entries for 19 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: decreased
classical genetics null
Allele: taz1-Δ
W303 cardiolipinde Taffin de Tilques M, et al. (2017) PMID:28188263
chemical compound accumulation: decreased
classical genetics null
Allele: taz1-Δ
W303 reactive oxygen speciesTreatment: microaerobic conditions
Details: decrease in ROS levels in the null mutant cultured under microaerobic conditions
Venkatraman K and Budin I (2024) PMID:39038656
chemical compound accumulation: decreased
classical genetics null
Allele: taz1-Δ
W303 cardiolipinTreatment: aerobic conditions
Details: ~50% reduction in cardiolipin levels in the null mutant cultured under aerobic conditions; returned to wt levels in a taz1-Δ ddl1-Δ double mutant
Venkatraman K and Budin I (2024) PMID:39038656
chemical compound accumulation: decreased
classical genetics null
Allele: taz1-Δ
W303 cardiolipinTreatment: microaerobic conditions
Details: ~75% reduction in cardiolipin levels in the null mutant cultured under microaerobic conditions
Venkatraman K and Budin I (2024) PMID:39038656
chemical compound accumulation: increased
classical geneticsnull
Allele: taz1-Δ
S288C 2-monolysocardiolipinDetails: in mitochondria
Beranek A, et al. (2009) PMID:19244244
chemical compound accumulation: increased
classical genetics null
Allele: taz1-Δ
W303 phosphatidylinositolde Taffin de Tilques M, et al. (2017) PMID:28188263
chemical compound accumulation: increased
classical genetics null
Allele: taz1-Δ
W303 reactive oxygen speciesde Taffin de Tilques M, et al. (2017) PMID:28188263
chemical compound accumulation: increased
classical genetics null
Allele: taz1-Δ
W303 phosphatidylglycerolTreatment: microaerobic conditions
Details: loss of cardiolipin is coupled with increased levels of phosphatidylglycerol in the null mutant cultured under microaerobic conditions
Venkatraman K and Budin I (2024) PMID:39038656
chromosome/plasmid maintenance: decreased
heterozygous diploid, systematic mutation setnull
Allele: taz1-Δ
S288CAssay: diploid bimater (BiM) assay
Details: haploinsufficiency results in chromosome instability (CIN); scored >= 2 standard deviations above the mean
Choy JS, et al. (2013) PMID:23825022
colony sectoring: increased
heterozygous diploid, systematic mutation setnull
Allele: taz1-Δ
S288CAssay: quantitative chromosome transmission fidelity (qCTF) assay
Details: >1.5 fold increase in mini-chromosome loss relative to wt, indicative of chromosome instability (CIN)
Zhu J, et al. (2015) PMID:25823586
Showing 1 to 10 of 36 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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