Phenotype Help

GCD7 / YLR291C 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
Essential gene; conditional mutants are defective in autophagy and in Golgi localization of reporter proteins; haploproficient but sensitive to starvation and oxidative stress

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.

19 entries for 12 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
cold sensitivity: increased
classical genetics reduction of function
Allele: gcd7-V341D
S288CTemperature: reduced temperature, 25 °C
Moon SL and Parker R (2018) PMID:30115954
colony sectoring: increased
classical geneticsconditional
Allele: gcd7-ts
S288CAssay: chromosome transmission fidelity (CTF) assay
Temperature: elevated temperature, 30 °C - 37 °C
Details: indicative of chromosome instability (CIN); score mild
Ben-Aroya S, et al. (2010) PMID:20174551
competitive fitness: decreased
competitive growth

fitness profiling of essential genes using hypomorphic DAmP alleles

reduction of functionS288CMedia: minimal medium
Details: Relative fitness score: 0.992
Breslow DK, et al. (2008) PMID:18622397
growth in exponential phase: decreased rate
classical genetics reduction of function
Allele: gcd7-V341D

eIF2Bβ-V341D corresponds to human EIF2Bβ-V316D; forms eIF2B complexes with reduced stability and lower activity

OtherDetails: eIF2Bβ-V341D exhibits reduced growth rate, defect in global translation
Richardson JP, et al. (2004) PMID:14993275
heat sensitivity: increased
large-scale surveyconditional
Allele: gcd7-ts
S288CTemperature: elevated temperature, 37 °C
Details: very slow growth
Ben-Aroya S, et al. (2008) PMID:18439903
heat sensitivity: increased
classical genetics reduction of function
Allele: gcd7-V341D
S288CTemperature: elevated temperature, 37 °C
Moon SL and Parker R (2018) PMID:30115954
hyperosmotic stress resistance: decreased
classical geneticsreduction of function
Allele: gcd7-201
Other1.25 M sodium chlorideGoossens A, et al. (2001) PMID:11408481
inviable
systematic mutation setnull
Allele: gcd7-Δ
S288CGiaever G, et al. (2002) PMID:12140549
inviable
classical geneticsnull
Allele: gcd7-Δ
OtherBushman JL, et al. (1993) PMID:8441423
protein/peptide accumulation: increased
Reporter: P-bodies
classical genetics reduction of function
Allele: gcd7-V341D
S288CMoon SL and Parker R (2018) PMID:30115954
Showing 1 to 10 of 19 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).


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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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