Difference between revisions of "YHR002W"
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|valign="top" nowrap bgcolor="{{SGDblue}}"| '''Coordinates''' | |valign="top" nowrap bgcolor="{{SGDblue}}"| '''Coordinates''' | ||
|nowrap| Chr VIII:108807..109880 | |nowrap| Chr VIII:108807..109880 | ||
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==Community Commentary== | ==Community Commentary== | ||
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==References== | ==References== | ||
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Revision as of 07:17, 30 January 2007
Share your knowledge...Edit this entry! <protect>
| Systematic name | YHR002W |
| Gene name | LEU5 |
| Aliases | |
| Feature type | ORF, Verified |
| Coordinates | Chr VIII:108807..109880 |
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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Contents
Community Commentary
About Community Commentary. Please share your knowledge!
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References
See Help:References on how to add references
See Help:Categories on how to add the wiki page for this gene to a Category </protect>
