YKL207W
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| Systematic name | YKL207W |
| Gene name | LRC3 |
| Aliases | |
| Feature type | ORF, Uncharacterized |
| Coordinates | Chr XI:48195..48956 |
| Primary SGDID | S000001690 |
Description of YKL207W: Putative protein of unknown function; non-essential gene; 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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