Phenotype Help

RAP1 / YNL216W 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
RAP1/YNL216W is an essential gene, null mutants are inviable; reduced function mutants have decreased fitness, long telomeres increased telomeric silencing, and are sensitive to DNA-damaging agent MMS; overexpression slows growth

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.

40 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
chromosome/plasmid maintenance: decreased
classical genetics overexpressionOtherDetails: chromosome loss rate ~20x higher than control
Conrad MN, et al. (1990) PMID:2225074
chromosome/plasmid maintenance: decreased
classical genetics reduction of function
Allele: rap1-17

P662L and a frameshift mutation creating a UGA (opal) stop codon at amino acid 664, resulting in a truncated protein of 663 amino acids

W303Details: elevated chromosome loss rates
Kyrion G, et al. (1992) PMID:1406688
competitive fitness: decreased
heterozygous diploid, competitive growth

genome-wide fitness profiling

null
Allele: rap1-Δ
S288CMedia: YPD
Details: Relative fitness score: 0.977
Deutschbauer AM, et al. (2005) PMID:15716499
competitive fitness: decreased
competitive growth

fitness profiling of essential genes using hypomorphic DAmP alleles

reduction of functionS288CMedia: minimal medium
Details: Relative fitness score: 0.976
Breslow DK, et al. (2008) PMID:18622397
haploinsufficient
heterozygous diploid, competitive growthnull
Allele: rap1-Δ
S288CDeutschbauer AM, et al. (2005) PMID:15716499
haploinsufficient
heterozygous diploid, systematic mutation set null
Allele: rap1-Δ
S288COhnuki S and Ohya Y (2018) PMID:29768403
haploproficient
heterozygous diploid, competitive growth

genome-wide fitness profiling

null
Allele: rap1-Δ
S288CMedia: turbidostat growth in FPM medium
Details: Relative growth score: 0.0029
Pir P, et al. (2012) PMID:22244311
inviable
systematic mutation setnull
Allele: rap1-Δ
S288CGiaever G, et al. (2002) PMID:12140549
metal resistance: decreased
systematic mutation set overexpressionS288C25 μM cadmium dichlorideDetails: exacerbates toxicity
Chakrabortee S, et al. (2016) PMID:27693355
metal resistance: decreased
systematic mutation set overexpressionS288C2 mM copper(II) sulfateDetails: exacerbates toxicity
Chakrabortee S, et al. (2016) PMID:27693355
Showing 1 to 10 of 40 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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