Phenotype Help

VHS1 / YDR247W 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.

28 entries for 16 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
homozygous diploid, systematic mutation set

glycogen accumulation in diploid mutant strains grown in microtiter plates

null
Allele: vhs1-Δ
S288C glycogenWilson WA, et al. (2002) PMID:12096123
chemical compound accumulation: increased
classical geneticsnull
Allele: vhs1-Δ
S288C glycogenTreatment: SC medium
Details: normal glycogen accumulation when grown on YPD medium
Wilson WA, et al. (2002) PMID:12096123
chemical compound accumulation: increased
classical genetics overexpressionW303 cadmium(2+)Treatment: cadmium dichloride, 50 µM
Details: increased accumulation of Cd2+, resulting in decreased Cd2+ tolerance
Zheng H, et al. (2024) PMID:39456809
chromosome/plasmid maintenance: decreased
systematic mutation setoverexpressionOtherAssay: a-like faker (ALF) assay
Details: dosage chromosome instability (dCIN) involving chromosome loss, rearrangement and/or gene conversion events
Duffy S, et al. (2016) PMID:27551064
chromosome/plasmid maintenance: decreased
heterozygous diploid, systematic mutation set overexpressionS288CDetails: mean frequency of loss of heterozygosity (LOH) at the CAN1 locus increased at least 2-fold; frequently accompanied by LOH at the MET6 locus indicating loss of the entire chr V
Tutaj H, et al. (2019) PMID:30244280
competitive fitness: decreased
systematic mutation setnull
Allele: vhs1-Δ
S288CMedia: glycerol medium, YPG
Qian W, et al. (2012) PMID:23103169
competitive fitness: increased
systematic mutation setnull
Allele: vhs1-Δ
S288CMedia: rich medium (YPD) w/6% ethanol, ETH
Qian W, et al. (2012) PMID:23103169
competitive fitness: increased
competitive growth

fitness profiling using complete deletion alleles

null
Allele: vhs1-Δ
S288CMedia: minimal medium
Details: Relative fitness score: 1.015
Breslow DK, et al. (2008) PMID:18622397
haploinsufficient
heterozygous diploid, competitive growthnull
Allele: vhs1-Δ
S288CTreatment: conditions that mimic Phase I of a batch fermentation, equivalent to ~14 hours after inoculation of a batch fermentation
Novo M, et al. (2013) PMID:24040173
haploproficient
heterozygous diploid, competitive growth

genome-wide fitness profiling

null
Allele: vhs1-Δ
S288CMedia: turbidostat growth in FPM medium
Details: Relative growth score: 0.0061
Pir P, et al. (2012) PMID:22244311
Showing 1 to 10 of 28 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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