Phenotype Help

TOF1 / YNL273W 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.

57 entries for 18 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
cell cycle progression in S phase: increased duration
classical geneticsnull
Allele: tof1-Δ
W303Tourrière H, et al. (2005) PMID:16137625
chromosome/plasmid maintenance: abnormal
homozygous diploidnull
Allele: tof1-Δ
S288CAssay: diploid bimater (BiM) assay
Details: increased frequency of mitotic chromosome loss
Daniel JA, et al. (2006) PMID:16157669
chromosome/plasmid maintenance: abnormal
homozygous diploidnull
Allele: tof1-Δ
S288CAssay: diploid bimater (BiM) assay
Details: indicative of chromosome instability (CIN); high confidence set; >= 5-fold increase over wildtype
Yuen KW, et al. (2007) PMID:17360454
chromosome/plasmid maintenance: abnormal
classical geneticsnull
Allele: tof1-Δ
S288CAssay: a-like faker (ALF) assay
Details: indicative of chromosome instability (CIN); high confidence set; 2- to 80-fold increase relative to wildtype
Yuen KW, et al. (2007) PMID:17360454
chromosome/plasmid maintenance: decreased
classical genetics null
Allele: tof1-Δ
Other15 ug/ml nocodazolePhase: G2/M phase
Details: precocious sister chromatid separation in ~13% of mitotic cells
Boginya A, et al. (2019) PMID:31222142
chromosome/plasmid maintenance: decreased
classical genetics null
Allele: tof1-Δ
S288CDetails: 113-fold increase in chromosome instability (CIN) relative to wt using a single-cell quantitative chromosome transmission fidelity (qCTF) assay that detects the loss of an ectopic chromosomal fragment of chrIII; CIN rate is suppressed by a helicase-dead mutant and by 32% when RRM3 is deleted
Gordon MR, et al. (2023) PMID:36350688
colony sectoring: increased
classical geneticsnull
Allele: tof1-Δ
S288CAssay: chromosome transmission fidelity (CTF) assay
Details: indicative of chromosome instability (CIN); high confidence set; severe sectoring phenotype
Yuen KW, et al. (2007) PMID:17360454
competitive fitness: decreased
competitive growth

fitness profiling using complete deletion alleles

null
Allele: tof1-Δ
S288CMedia: minimal medium
Details: Relative fitness score: 0.955
Breslow DK, et al. (2008) PMID:18622397
competitive fitness: decreased
systematic mutation setnull
Allele: tof1-Δ
S288CMedia: rich medium (YPD) w/6% ethanol, ETH
Qian W, et al. (2012) PMID:23103169
competitive fitness: decreased
systematic mutation setnull
Allele: tof1-Δ
S288CMedia: YPD
Qian W, et al. (2012) PMID:23103169
Showing 1 to 10 of 57 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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