Phenotype Help

SAR1 / YPL218W 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.

17 entries for 10 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
competitive fitness: decreased
competitive growth

fitness profiling of essential genes using hypomorphic DAmP alleles

reduction of functionS288CMedia: minimal medium
Details: Relative fitness score: 0.956
Breslow DK, et al. (2008) PMID:18622397
endoplasmic reticulum morphology: abnormal
classical geneticsconditionalOtherTemperature: elevated temperature, 37 °C
Details: ER membrane accumulation
Yamanushi T, et al. (1996) PMID:8889833
haploinsufficient
heterozygous diploid, competitive growthnull
Allele: sar1-Δ
S288CTreatment: conditions that mimic Phase II of a batch fermentation, equivalent to ~22 hours after inoculation of a batch fermentation
Novo M, et al. (2013) PMID:24040173
inviable
systematic mutation setnull
Allele: sar1-Δ
S288CGiaever G, et al. (2002) PMID:12140549
inviable
classical genetics null
Allele: sar1-Δ
OtherNakańo A and Muramatsu M (1989) PMID:2512296
mitochondrial morphology: abnormal
classical geneticsoverexpressionOtherTemperature: elevated temperature, 37 °C
Details: mitochondria became thinner and inner mitochondrial membranes are aberrant
Ackema KB, et al. (2016) PMID:27101143
mitochondrial morphology: abnormal
classical geneticsconditional
Allele: sar1-D32G

D32G; GDP-restricted mutant

OtherTemperature: elevated temperature, 37 °C
Details: lusters of mitochondrial fragments are observed, size of ER-mitochondrial contacts is increased, and cristae are aberrant or absent
Ackema KB, et al. (2016) PMID:27101143
mitochondrial morphology: abnormal
classical geneticsconditional
Allele: sar1-D32G

D32G; GDP-restricted mutant

OtherTemperature: permissive temperature, 23 °C
Details: globular mitochondrial structures, and less tubular networks are observed
Ackema KB, et al. (2016) PMID:27101143
nuclear morphology: abnormal
classical genetics null
Allele: sar1-Δ
S288CHorikawa K, et al. (2019) PMID:31406088
protein/peptide accumulation: increased
Reporter: precursor carboxypeptidase Y

proCPY (pCPY)

classical geneticsdominant negativeOtherNakano A, et al. (1994) PMID:7822237
Showing 1 to 10 of 17 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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