Phenotype Help

PLP1 / YDR183W 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 11 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 through the G2/M phase transition: normal rate
classical geneticsnull
Allele: plp1-Δ
OtherDetails: wild-type percentage of large-budded cells
Lacefield S, et al. (2006) PMID:16582437
chemical compound accumulation: increased
systematic mutation setnull
Allele: plp1-Δ
S288C cadmium cationYu D, et al. (2012) PMID:23151179
competitive fitness: decreased
competitive growth

fitness profiling using complete deletion alleles

null
Allele: plp1-Δ
S288CMedia: minimal medium
Details: Relative fitness score: 0.975
Breslow DK, et al. (2008) PMID:18622397
competitive fitness: decreased
systematic mutation setnull
Allele: plp1-Δ
S288CMedia: synthetic oak exudate medium, OAK
Qian W, et al. (2012) PMID:23103169
protein activity: increased
Reporter: metal reductase
systematic mutation set

cell surface metal reductase activity quantified using BPS and scoring colonies for red color

null
Allele: plp1-Δ
S288CDong K, et al. (2013) PMID:23959798
protein/peptide accumulation: abnormal
Reporter: Tub2p
classical geneticsnull
Allele: plp1-Δ
OtherDetails: decreased accumulation of tubulin heterodimers
Lacefield S and Solomon F (2003) PMID:14573467
resistance to chemicals: decreased
homozygous diploid, systematic mutation setnull
Allele: plp1-Δ
S288C2 mM sorbateMedia: pH 4.5
Mollapour M, et al. (2004) PMID:15334557
resistance to chemicals: decreased
systematic mutation setnull
Allele: plp1-Δ
S288C3.2 uM bleomycinKapitzky L, et al. (2010) PMID:21179023
resistance to chemicals: decreased
systematic mutation setnull
Allele: plp1-Δ
S288C1 uM myriocinFröhlich F, et al. (2015) PMID:26357016
resistance to chemicals: decreased
homozygous diploid, competitive growth null
Allele: plp1-Δ
S288C3.05 μM epoxiconazoleDetails: sensitive at the IC50 concentration of epoxiconazole relative to wt
Guan M, et al. (2020) PMID:32919014
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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