Phenotype Help

BDH2 / YAL061W 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 reference strain S288C; null mutant displays decreased competitive fitness and sensitivity to hyperosmotic stress; heterozygous null mutant displays decreased fitness and decreased resistance to starvation

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.

12 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
chemical compound accumulation: increased
classical genetics overexpressionOther tetramethylpyrazineCui DY, et al. (2020) PMID:33324376
chronological lifespan: decreased
systematic mutation set null
Allele: bdh2-Δ
S288CCampos SE, et al. (2018) PMID:29575540
competitive fitness: decreased
competitive growth

fitness profiling using complete deletion alleles

null
Allele: bdh2-Δ
S288CMedia: minimal medium
Details: Relative fitness score: 0.974
Breslow DK, et al. (2008) PMID:18622397
haploinsufficient
heterozygous diploid, competitive growth

genome-wide fitness profiling

null
Allele: bdh2-Δ
S288CMedia: turbidostat growth in FPM medium
Details: Relative growth score: -0.008
Pir P, et al. (2012) PMID:22244311
heat sensitivity: decreased
systematic mutation set

high throughput heat ramp cell death assay

null
Allele: bdh2-Δ
S288CTemperature: elevated temperature
Details: ramp temperature from ambient to 30 deg C immediately, hold 1 min at 30 deg C, ramp temperature from 30 deg C to 62 deg C over 20 min, return to ambient
Teng X, et al. (2011) PMID:21814286
hyperosmotic stress resistance: decreased
systematic mutation setnull
Allele: bdh2-Δ
S288C1 M sodium chlorideYoshikawa K, et al. (2009) PMID:19054128
resistance to chemicals: decreased
systematic mutation setnull
Allele: bdh2-Δ
S288C vanillinIshida Y, et al. (2016) PMID:27458450
resistance to chemicals: increased
large-scale survey

variomic library screening of ~10,000 alleles for each gene

unspecifiedS288C100 ng/ml cycloheximideHuang Z, et al. (2013) PMID:23416056
starvation resistance: decreased
heterozygous diploid, competitive growth

pooled mutant strains were subjected to low nutrient stress, then dead cells were separated and their mutations identified

null
Allele: bdh2-Δ
S288CDavey HM, et al. (2012) PMID:22356628
stress resistance: decreased
systematic mutation set null
Allele: bdh2-Δ
S288CTreatment: visible light, 400-700 nm
Details: sensitive to visible light induced stress; high confidence
Molin M, et al. (2020) PMID:33198745
Showing 1 to 10 of 12 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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