AIM10 / YER087W 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 heat sensitive, has a vegetative growth defect, a respiratory growth defect and displays reduced competitive fitness in various media; null mutant has a decreased ability to utilize the carbon source galactose and the nitrogen sources, glutamine and proline; null mutant displays a decreased frequency of spontaneous mitochondrial genome loss but an elevated nuclear mutation frequency; null mutant has a small cell size, decreased chronological lifespan, decreased desiccation resistance, and displays a reduction in the number of lipid particles per cell; heterozygous null mutant is haploinsufficient

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.

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