Phenotype Help

NUP133 / YKR082W 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.

78 entries for 30 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
bud morphology: abnormal
systematic mutation setnull
Allele: nup133-Δ
S288CDetails: bud is abnormally elongated
Watanabe M, et al. (2009) PMID:19466415
chemical compound accumulation: abnormal
systematic mutation setnull
Allele: nup133-Δ
S288C alpha-amino acidDetails: Significantly altered free amino acid profile (X^2- test adjusted p < 0.01), showing 2 simultaneous amino acid changes (Z-test, adjusted p < 0.01)
Mülleder M, et al. (2016) PMID:27693354
chemical compound accumulation: increased
homozygous diploidnull
Allele: nup133-Δ
S288C0.1 mM potassium tellurite, tellurium atomOttosson LG, et al. (2010) PMID:20675578
chemical compound accumulation: increased
systematic mutation setnull
Allele: nup133-Δ
S288C prolineMülleder M, et al. (2016) PMID:27693354
chemical compound accumulation: increased
systematic mutation setnull
Allele: nup133-Δ
S288C glutamate(1-)Mülleder M, et al. (2016) PMID:27693354
chitin deposition: increased
systematic mutation setnull
Allele: nup133-Δ
S288CDetails: Chitin level (nmole GlcNAc/mg dry weight): 25.7
Lesage G, et al. (2005) PMID:15715908
chromosome/plasmid maintenance: abnormal
homozygous diploidnull
Allele: nup133-Δ
S288CDetails: loss of heterozygosity at the SAM2 locus increased 20-fold or greater, at MET15 increased 2-6 fold, but not changed at MAT
Andersen MP, et al. (2008) PMID:18562670
chromosome/plasmid maintenance: abnormal
classical geneticsnull
Allele: nup133-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
colony sectoring: increased
classical geneticsnull
Allele: nup133-Δ
S288CAssay: chromosome transmission fidelity (CTF) assay
Details: indicative of chromosome instability (CIN); high confidence set; mild sectoring phenotype
Yuen KW, et al. (2007) PMID:17360454
competitive fitness: decreased
homozygous diploid, competitive growth

genome-wide fitness profiling

null
Allele: nup133-Δ
S288CMedia: YPD
Details: Relative fitness score: 0.875
Deutschbauer AM, et al. (2005) PMID:15716499
Showing 1 to 10 of 78 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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