YBR108W
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| Systematic name | YBR108W |
| Gene name | AIM3 |
| Aliases | |
| Feature type | ORF, Uncharacterized |
| Coordinates | Chr II:454816..457659 |
| Primary SGDID | S000000312 |
Description of YBR108W: Protein interacting with Rsv167p; null mutant displays decreased frequency of mitochondrial genome loss (petite formation) and severe growth defect in minimal glycerol media[1][2]
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Contents
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References
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- ↑ Hess D, et al. (2008) Integrating computation and experimentation to discover novel mitochondrial biology Science SGD PMID
- ↑ Germann M, et al. (2005) Characterizing the sphingolipid signaling pathway that remediates defects associated with loss of the yeast amphiphysin-like orthologs, Rvs161p and Rvs167p. J Biol Chem 280(6):4270-8 SGD PMID 15561700
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