YOR291W
Revision as of 08:18, 30 January 2007 by SGDwikiBot (talk | contribs) (Automated import of articles)
Share your knowledge...Edit this entry! <protect>
Systematic name | YOR291W |
Gene name | |
Aliases | |
Feature type | ORF, Uncharacterized |
Coordinates | Chr XV:861174..865592 |
Description of YOR291W: Hypothetical protein
</protect>
Contents
[hide]Community Commentary
About Community Commentary. Please share your knowledge!
Alleles, Strains, and Phenotypes
Complete Deletion
Phenotype(s): No Phenotype, Viable
No obvious phenotypes were detected upon deletion of YOR291w with a KanMX deletion cassette. The deletion was confirmed by PCR. [1] [2]
Phenotype(s): No Phenotype, Viable
No obvious phenotypes were detected upon deletion of YOR291w with a KanMX deletion cassette. The deletion was confirmed by PCR. [1] [2]
<protect>
References
See Help:References on how to add references
- ↑ Jump up to: 1.0 1.1 Cronin SR, et al. (2000) Regulation of HMG-CoA reductase degradation requires the P-type ATPase Cod1p/Spf1p. J Cell Biol 148(5):915-24 SGD PMID 10704442
- ↑ Jump up to: 2.0 2.1 submitted by Stephen R. Cronin on 2003-06-13
See Help:Categories on how to add the wiki page for this gene to a Category </protect>