Phenotype Help

ALG8 / YOR067C 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; null mutant is sensitive to reducing agents such as mercaptoethanol and DTT and displays under-glycosylation of secreted proteins; in large-scale studies, the null mutant requires myo-inositol, displays rounded cell shape and decreased competitive fitness, and has altered sensitivity to a variety of chemicals

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.

61 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
auxotrophy
homozygous diploid, systematic mutation setnull
Allele: alg8-Δ
S288C myo-inositolVilla-García MJ, et al. (2011) PMID:21136082
budding pattern: abnormal
homozygous diploid, systematic mutation setnull
Allele: alg8-Δ
S288CDetails: unipolar budding pattern
Ni L and Snyder M (2001) PMID:11452010
cell shape: abnormal
homozygous diploid, large-scale surveynull
Allele: alg8-Δ
S288CDetails: round cell shape; moderate defect
Ni L and Snyder M (2001) PMID:11452010
chemical compound accumulation: abnormal
systematic mutation setnull
Allele: alg8-Δ
S288C alpha-amino acidDetails: Significantly altered free amino acid profile (X^2- test p < 0.01), showing 1 simultaneous amino acid change (Z-test, adjusted p < 0.01)
Mülleder M, et al. (2016) PMID:27693354
chemical compound accumulation: decreased
systematic mutation setnull
Allele: alg8-Δ
S288C magnesium cationYu D, et al. (2012) PMID:23151179
chemical compound accumulation: increased
systematic mutation setnull
Allele: alg8-Δ
S288C sodium(1+)Yu D, et al. (2012) PMID:23151179
chemical compound accumulation: increased
systematic mutation setnull
Allele: alg8-Δ
S288C glutamate(1-)Mülleder M, et al. (2016) PMID:27693354
chromosome/plasmid maintenance: decreased
heterozygous diploid, systematic mutation setnull
Allele: alg8-Δ
S288CAssay: diploid bimater (BiM) assay
Details: haploinsufficiency results in chromosome instability (CIN); scored >= 2 standard deviations above the mean
Choy JS, et al. (2013) PMID:23825022
chronological lifespan: decreased
competitive growth

competitive survival of mixed stationary phase co-cultures

null
Allele: alg8-Δ
S288CGaray E, et al. (2014) PMID:24586198
competitive fitness: decreased
systematic mutation set

fitness profiling after 5 generations

null
Allele: alg8-Δ
S288C10 uM nystatinGiaever G, et al. (2002) PMID:12140549
Showing 1 to 10 of 61 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).


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