ARG2 / YJL071W 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

Non-essential gene; null mutant is auxotrophic for arginine and is unable to use allantoin as nitrogen source; null mutant has decreased competitive fitness in synthetic media but increased fitness in media containing glycerol or ethanol; null has decreased resistance to alpha-synuclein expression, and accumulates increased reactive oxygen species (ROS), while overexpression decreases the accumulation of ROS associated associated with alpha-synuclein expression; systematic null mutant has decreased telomere length and increased metal reductase activity

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.

20 entries for 16 phenotypes

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).

Resources