Phenotype Help

MIC60 / YKR016W 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.

46 entries for 19 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 using complete deletion alleles

null
Allele: mic60-Δ
S288CMedia: minimal medium
Details: Relative fitness score: 0.933
Breslow DK, et al. (2008) PMID:18622397
competitive fitness: decreased
systematic mutation setnull
Allele: mic60-Δ
S288C ethanolQian W, et al. (2012) PMID:23103169
competitive fitness: decreased
systematic mutation setnull
Allele: mic60-Δ
S288CMedia: glycerol medium, YPG
Qian W, et al. (2012) PMID:23103169
competitive fitness: decreased
systematic mutation setnull
Allele: mic60-Δ
S288CMedia: rich medium (YPD) w/6% ethanol, ETH
Qian W, et al. (2012) PMID:23103169
competitive fitness: decreased
systematic mutation setnull
Allele: mic60-Δ
S288CMedia: synthetic complete medium, SC
Qian W, et al. (2012) PMID:23103169
invasive growth: increased
homozygous diploid, systematic mutation setoverexpressionSigma1278bMedia: nitrogen-sufficient medium
Details: agar invasion score: 0.98; enhanced pseudohyphal growth, based on elevated invasiveness
Shively CA, et al. (2013) PMID:23410832
mitochondrial genome maintenance: abnormal
large-scale surveynull
Allele: mic60-Δ
S288CDetails: decreased frequency of spontaneous mitochondrial genome loss
Hess DC, et al. (2009) PMID:19300474
mitochondrial genome maintenance: abnormal
classical genetics null
Allele: mic60-Δ
OtherDetails: decreased number of mitochondrial nucleoids, although mtDNA concentration is not reduced
Seel A, et al. (2023) PMID:37679564
mitochondrial morphology: abnormal
classical geneticsoverexpressionW303Details: number of crista junctions increased 2- to 3-fold; branching of crista increased 17-fold
Rabl R, et al. (2009) PMID:19528297
mitochondrial morphology: abnormal
classical geneticsrepressibleW303Details: progressive decrease in number of crista junctions and branches
Rabl R, et al. (2009) PMID:19528297
Showing 1 to 10 of 46 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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