Difference between revisions of "YBR108W"
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| − | '''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<ref name='S000124966'>Hess D, et al. (2008) | + | '''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<ref name='S000124966'>Hess D, et al. (2008) {{SGDpaper|S000124966}} PMID </ref><ref name='S000080197'>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 |
{{SGDpaper|S000080197}} PMID 15561700</ref> | {{SGDpaper|S000080197}} PMID 15561700</ref> | ||
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Revision as of 13:05, 6 June 2008
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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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