Phenotype Help

HOT1 / YMR172W 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.

12 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
chemical compound accumulation: abnormal
systematic mutation setnull
Allele: hot1-Δ
S288C alpha-amino acidDetails: Significantly altered free amino acid profile (X^2- test adjusted p < 0.01), showing 2 simultaneous amino acid changes (Z-test, adjusted p < 0.01)
Mülleder M, et al. (2016) PMID:27693354
chemical compound accumulation: decreased
systematic mutation setnull
Allele: hot1-Δ
S288C N(2)-acetyl-L-ornithineCooper SJ, et al. (2010) PMID:20610602
chemical compound accumulation: increased
systematic mutation setnull
Allele: hot1-Δ
S288C alanineMülleder M, et al. (2016) PMID:27693354
chemical compound accumulation: increased
systematic mutation setnull
Allele: hot1-Δ
S288C threonineMülleder M, et al. (2016) PMID:27693354
competitive fitness: decreased
competitive growth

fitness profiling using complete deletion alleles

null
Allele: hot1-Δ
S288CMedia: minimal medium
Details: Relative fitness score: 0.922
Breslow DK, et al. (2008) PMID:18622397
killer toxin resistance: increased
homozygous diploidnull
Allele: hot1-Δ
S288CTreatment: HM-1
Miyamoto M, et al. (2012) PMID:23065846
metal resistance: increased
systematic mutation set null
Allele: hot1-Δ
S288C lithium(1+)Treatment: lithium chloride, 200 mM
Details: null mutants exhibiting growth below 110% at 200 mM LiCl were classified as having a low level of resistance; screen consisted of a 4 step approach including qualitative assessment on Li-agar plates, liquid microplate assessment, tertiary screening in liquid and a quaternary screen using Li2SO4, followed by classification based on the degree of sensitivity
Fierling N, et al. (2024) PMID:38142127
resistance to chemicals: decreased
systematic mutation setnull
Allele: hot1-Δ
S288C1 uM myriocinFröhlich F, et al. (2015) PMID:26357016
sporulation: normal
homozygous diploid, systematic mutation set

Visual inspection by light microscopy

null
Allele: hot1-Δ
SK1Rabitsch KP, et al. (2001) PMID:11470404
vacuolar morphology: abnormal
systematic mutation set

screen all non-essential genes for inability to fragment vacuoles in response to salt addition

null
Allele: hot1-Δ
S288C0.4 M sodium chlorideDetails: small defect in vacuolar fragmentation
Michaillat L and Mayer A (2013) PMID:23383298
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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