Difference between revisions of "YDR375C"
SGDwikiBot (talk | contribs) (Automated import of articles) |
SGDwikiBot (talk | contribs) (Automated import of articles) |
||
Line 13: | Line 13: | ||
|- | |- | ||
|valign="top" nowrap bgcolor="{{SGDblue}}"| '''Coordinates''' | |valign="top" nowrap bgcolor="{{SGDblue}}"| '''Coordinates''' | ||
− | |nowrap| Chr IV: | + | |nowrap| Chr IV:1226536..1225166 |
|- | |- | ||
|valign="top" nowrap bgcolor="{{SGDblue}}"| '''Primary SGDID''' || S000002783 | |valign="top" nowrap bgcolor="{{SGDblue}}"| '''Primary SGDID''' || S000002783 |
Revision as of 14:05, 3 February 2011
Share your knowledge...Edit this entry! <protect>
Systematic name | YDR375C |
Gene name | BCS1 |
Aliases | |
Feature type | ORF, Verified |
Coordinates | Chr IV:1226536..1225166 |
Primary SGDID | S000002783 |
Description of YDR375C: Mitochondrial protein of the AAA ATPase family; has ATP-dependent chaperone activity; required for assembly of Rip1p and Qcr10p into cytochrome bc(1) complex; mutations in human homolog BCS1L are linked to neonatal mitochondrial diseases[1][2]
</protect>
Contents
Community Commentary
About Community Commentary. Please share your knowledge!
<protect>
References
See Help:References on how to add references
- ↑ Cruciat CM, et al. (1999) Bcs1p, an AAA-family member, is a chaperone for the assembly of the cytochrome bc(1) complex. EMBO J 18(19):5226-33 SGD PMID 10508156
- ↑ Tuppen HA, et al. (2010) Long-term survival of neonatal mitochondrial complex III deficiency associated with a novel BCS1L gene mutation. Mol Genet Metab 100(4):345-8 SGD PMID 20472482
See Help:Categories on how to add the wiki page for this gene to a Category </protect>