Phenotype Help

ASP1 / YDR321W 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.


Summary
Non-essential gene; in competitive-growth studies null mutant shows reduced fitness; in systematic studies null mutant has lower rate of utilization of ammonium as nitrogen source

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.

7 entries for 7 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
chemical compound accumulation: increased
systematic mutation setnull
Allele: asp1-Δ
S288C asparagineMülleder M, et al. (2016) PMID:27693354
competitive fitness: decreased
competitive growth

fitness profiling using complete deletion alleles

null
Allele: asp1-Δ
S288CMedia: minimal medium
Details: Relative fitness score: 0.985
Breslow DK, et al. (2008) PMID:18622397
oxidative stress resistance: increased
competitive growth null
Allele: asp1-Δ
S288C1 mM paraquatHelsen J, et al. (2020) PMID:32658971
resistance to chemicals: decreased
homozygous diploid, systematic mutation setnull
Allele: asp1-Δ
S288C benzo[a]pyreneO'Connor ST, et al. (2012) PMID:23403841
utilization of nitrogen source: decreased rate
systematic mutation set

prototrophic version of yeast deletion collection

null
Allele: asp1-Δ
S288C ammoniumVanderSluis B, et al. (2014) PMID:24721214
vacuolar morphology: abnormal
systematic mutation set

screen all non-essential genes for inability to fragment vacuoles in response to salt addition

null
Allele: asp1-Δ
S288C0.4 M sodium chlorideDetails: small defect in vacuolar fragmentation
Michaillat L and Mayer A (2013) PMID:23383298
viable
systematic mutation setnull
Allele: asp1-Δ
S288CGiaever G, et al. (2002) PMID:12140549
Showing 1 to 7 of 7 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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