Phenotype Help

TRM82 / YDR165W 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.

15 entries for 12 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
chronological lifespan: decreased
competitive growth

competitive survival of mixed stationary phase co-cultures

null
Allele: trm82-Δ
S288CGaray E, et al. (2014) PMID:24586198
competitive fitness: decreased
competitive growth

fitness profiling using complete deletion alleles

null
Allele: trm82-Δ
S288CMedia: minimal medium
Details: Relative fitness score: 0.987
Breslow DK, et al. (2008) PMID:18622397
haploproficient
heterozygous diploid, competitive growth

genome-wide fitness profiling

null
Allele: trm82-Δ
S288CMedia: turbidostat growth in FPM medium
Details: Relative growth score: 0.0072
Pir P, et al. (2012) PMID:22244311
heat sensitivity: increased
classical geneticsconditional
Allele: trm82-K223L

corresponds to to human WDR4-R170L mutation (NM_033661.4:c.509G>T; p.Arg170Leu) associated with microcephalic primordial dwarfism

S288CTemperature: elevated temperature, 39 °C
Details: growth was assayed in a trm82 trm4 double null mutant background to amplify growth defects
Shaheen R, et al. (2015) PMID:26416026
oxidative stress resistance: increased
homozygous diploid, competitive growthnull
Allele: trm82-Δ
S288C3 mM hydrogen peroxideBrown JA, et al. (2006) PMID:16738548
resistance to chemicals: decreased
systematic mutation setnull
Allele: trm82-Δ
S288C15 ug/ml 5-fluorouracilGustavsson M and Ronne H (2008) PMID:18314501
resistance to chemicals: decreased
classical geneticsnull
Allele: trm82-Δ
S288C1 ug/mL 5-fluorouracilTemperature: elevated temperature, 38 °C
Gustavsson M and Ronne H (2008) PMID:18314501
resistance to chemicals: decreased
homozygous diploid, systematic mutation setnull
Allele: trm82-Δ
S288C8 mM methylglyoxalHoon S, et al. (2011) PMID:22384333
resistance to chemicals: decreased
homozygous diploid, competitive growth null
Allele: trm82-Δ
S288C60 μg/ml sodium disulfiteDetails: sensitive to sulfite concentrations of about 34 μg/ml with a log(FC)<-5
Valero E, et al. (2020) PMID:31638329
RNA modification: absent
Reporter: tRNA-Phe
classical geneticsconditional
Allele: trm82-K223L

corresponds to to human WDR4-R170L mutation (NM_033661.4:c.509G>T; p.Arg170Leu) associated with microcephalic primordial dwarfism

S288CTemperature: elevated temperature, 37 °C
Details: tRNA-Phe lacks m7G46 methylation
Shaheen R, et al. (2015) PMID:26416026
Showing 1 to 10 of 15 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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