Phenotype Help

PRS3 / YHL011C 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
PRS3/YHL011C is a non-essential gene; null mutants are viable, slow-growing, and exhibit a variety of phenotypic abnormalities including decreased budding index and abnormal budding pattern, indicating disruptions in cell division; increased duration of cell cycle progression in G1, suggesting delays in cell cycle progression; abnormal cell shape and cellular morphology, and decreased cell size, indicating alterations in growth regulation; diminished competitive fitness, making these mutants less viable in competitive environments; decreased desiccation resistance, making them more vulnerable to dry conditions; slow fermentative growth, indicating impaired energy production under anaerobic conditions, and decreased respiratory growth, indicating impaired energy production under aerobic conditions; decreased hyperosmotic stress resistance and innate thermotolerance, suggesting heightened sensitivity to osmotic and temperature stress; decreased killer toxin resistance, making these mutants more susceptible to certain toxins; reduced sporulation efficiency, affecting reproductive success; decreased telomere length, which may impact chromosome stability and cellular aging; and decreased UV resistance, making these mutants more vulnerable to UV-induced damage.

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.


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.

Gene Phenotype Experiment Type Mutant Information Strain Background Chemical Details Reference

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.


Resources