Difference between revisions of "YPL172C"
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|valign="top" nowrap bgcolor="{{SGDblue}}"| '''Coordinates''' | |valign="top" nowrap bgcolor="{{SGDblue}}"| '''Coordinates''' | ||
|nowrap| Chr XVI:225740..224352 | |nowrap| Chr XVI:225740..224352 | ||
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==Community Commentary== | ==Community Commentary== | ||
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==References== | ==References== | ||
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Revision as of 07:18, 30 January 2007
Share your knowledge...Edit this entry! <protect>
| Systematic name | YPL172C |
| Gene name | COX10 |
| Aliases | |
| Feature type | ORF, Verified |
| Coordinates | Chr XVI:225740..224352 |
Description of YPL172C: Heme A:farnesyltransferase, catalyzes the first step in the conversion of protoheme to the heme A prosthetic group required for cytochrome c oxidase activity; human ortholog is associated with mitochondrial disorders[1][2]
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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
- ↑ Glerum DM and Tzagoloff A (1994) Isolation of a human cDNA for heme A:farnesyltransferase by functional complementation of a yeast cox10 mutant. Proc Natl Acad Sci U S A 91(18):8452-6 SGD PMID 8078902
- ↑ Valnot I, et al. (2000) A mutation in the human heme A:farnesyltransferase gene (COX10 ) causes cytochrome c oxidase deficiency. Hum Mol Genet 9(8):1245-9 SGD PMID 10767350
See Help:Categories on how to add the wiki page for this gene to a Category </protect>
