Phenotype Help

RSA4 / YCR072C 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.

13 entries for 8 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
competitive fitness: normal
competitive growth

fitness profiling of essential genes using hypomorphic DAmP alleles

reduction of functionS288CMedia: minimal medium
Details: Relative fitness score: 1.000
Breslow DK, et al. (2008) PMID:18622397
haploinsufficient
heterozygous diploid, systematic mutation set null
Allele: rsa4-Δ
S288COhnuki S and Ohya Y (2018) PMID:29768403
heat sensitivity: increased
large-scale surveyconditional
Allele: rsa4-ts
S288CTemperature: elevated temperature, 37 °C
Details: very slow growth
Ben-Aroya S, et al. (2008) PMID:18439903
inviable
systematic mutation setnull
Allele: rsa4-Δ
S288CGiaever G, et al. (2002) PMID:12140549
inviable
classical geneticsdominant negative
Allele: rsa4-E114D

N-terminal ubiquitin like domain, MIDAS ion coordination site mutated

W303Ulbrich C, et al. (2009) PMID:19737519
inviable
classical geneticsunspecified
Allele: rsa4-E114A

N-terminal ubiquitin like domain, MIDAS ion coordination site mutated

W303Ulbrich C, et al. (2009) PMID:19737519
inviable
classical geneticsoverexpression
Allele: rsa4-E114D

N-terminal ubiquitin like domain, MIDAS ion coordination site mutated; dominant negative

W303Ulbrich C, et al. (2009) PMID:19737519
protein/peptide accumulation: decreased
Reporter: 60S ribosomal subunit
classical geneticsoverexpression
Allele: rsa4-E114D

N-terminal ubiquitin like domain, MIDAS ion coordination site mutated; dominant negative

W303Details: reduction in mature 60S ribosomal subunit, relative to 40S and the appearance of half-mer polysomes
Ulbrich C, et al. (2009) PMID:19737519
protein/peptide distribution: abnormal
Reporter: pre-60S ribosomal subunit
classical geneticsoverexpression
Allele: rsa4-E114D

N-terminal ubiquitin like domain, MIDAS ion coordination site mutated; dominant negative

W303Details: accumulation of pre-60S ribosomal subunits in the nucleoplasm
Ulbrich C, et al. (2009) PMID:19737519
resistance to chemicals: decreased
systematic mutation setconditional
Allele: rsa4-5001
S288C2 ug/mL camptothecinForster DT, et al. (2022) PMID:36192463
Showing 1 to 10 of 13 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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