Phenotype Help

NRT1 / YOR071C 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 16 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: nrt1-Δ
S288C alpha-amino acidDetails: Significantly altered free amino acid profile (X^2- test p < 0.01), showing 1 simultaneous amino acid change (Z-test, adjusted p < 0.01)
Mülleder M, et al. (2016) PMID:27693354
chemical compound accumulation: decreased
classical geneticsnull
Allele: nrt1-Δ
S288C NAD(+)Media: nicotinic acid free medium supplemented with nicotinamide riboside
Details: reduction in the nicotinamide riboside induced increase in NAD+; 83%
Belenky PA, et al. (2008) PMID:18258590
chemical compound accumulation: increased
systematic mutation setnull
Allele: nrt1-Δ
S288C glycineMülleder M, et al. (2016) PMID:27693354
chemical compound excretion: increased
classical geneticsnull
Allele: nrt1-Δ
S288C N-ribosylnicotinamideLu SP and Lin SJ (2011) PMID:21349851
chronological lifespan: increased
homozygous diploid, large-scale surveynull
Allele: nrt1-Δ
S288CBurtner CR, et al. (2011) PMID:21447998
competitive fitness: decreased
competitive growth overexpressionS288CDetails: decreased abundance within the barFLEX overexpression collection arrayed after 20 generations of pooled growth
Douglas AC, et al. (2012) PMID:23050238
competitive fitness: increased
competitive growth

fitness profiling using complete deletion alleles

null
Allele: nrt1-Δ
S288CMedia: minimal medium
Details: Relative fitness score: 1.006
Breslow DK, et al. (2008) PMID:18622397
heat sensitivity: decreased
systematic mutation set

high throughput heat ramp cell death assay

null
Allele: nrt1-Δ
S288CTemperature: elevated temperature
Details: ramp temperature from ambient to 30 deg C immediately, hold 1 min at 30 deg C, ramp temperature from 30 deg C to 62 deg C over 20 min, return to ambient
Teng X, et al. (2011) PMID:21814286
nutrient uptake: absent
Reporter: nicotinamide riboside
classical geneticsnull
Allele: nrt1-Δ
S288CBelenky PA, et al. (2008) PMID:18258590
nutrient utilization: decreased
Reporter: nicotinamide riboside
classical geneticsnull
Allele: nrt1-Δ
S288CBelenky PA, et al. (2008) PMID:18258590
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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