AIM7 / YDR063W 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 has decreased competitive fitness in minimal medium, but increased fitness in rich medium containing 6% ethanol; null mutant has a reduced frequency of spontaneous mitochondrial genome loss; haploinsufficiency in the heterozygous diploid null mutant results in chromosomal instability; null mutant has increased innate thermotolerance in stationary phase; DL:LL dityrosine ratio is altered in spores of the null mutant

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

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