YHR002W
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Systematic name | YHR002W |
Gene name | LEU5 |
Aliases | |
Feature type | ORF, Verified |
Coordinates | Chr VIII:108812..109885 |
Primary SGDID | S000001044 |
Description of YHR002W: Mitochondrial carrier protein involved in the accumulation of CoA in the mitochondrial matrix; homolog of human Graves disease protein; does not encode an isozyme of Leu4p, as first hypothesized[1]
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