Difference between revisions of "YHR002W"
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|valign="top" nowrap bgcolor="{{SGDblue}}"| '''Coordinates''' | |valign="top" nowrap bgcolor="{{SGDblue}}"| '''Coordinates''' | ||
| − | |nowrap| Chr VIII: | + | |nowrap| Chr VIII:108812..109885 |
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|valign="top" nowrap bgcolor="{{SGDblue}}"| '''Primary SGDID''' || S000001044 | |valign="top" nowrap bgcolor="{{SGDblue}}"| '''Primary SGDID''' || S000001044 | ||
Revision as of 13:05, 3 February 2011
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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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