YGL168W
Revision as of 07:45, 23 January 2012 by SGDwikiBot (talk | contribs) (Automated import of articles)
Share your knowledge...Edit this entry! <protect>
Systematic name | YGL168W |
Gene name | HUR1 |
Aliases | |
Feature type | ORF, Verified |
Coordinates | Chr VII:187464..187796 |
Primary SGDID | S000003136 |
Description of YGL168W: Protein of unknown function; reported null mutant phenotype of hydroxyurea sensitivity may be due to effects on overlapping PMR1 gene[1][2][3]
</protect>
Contents
[hide]Community Commentary
About Community Commentary. Please share your knowledge!
<protect>
References
See Help:References on how to add references
- Jump up ↑ Askree SH, et al. (2004) A genome-wide screen for Saccharomyces cerevisiae deletion mutants that affect telomere length. Proc Natl Acad Sci U S A 101(23):8658-63 SGD PMID 15161972
- Jump up ↑ Jordan PW, et al. (2007) Novel roles for selected genes in meiotic DNA processing. PLoS Genet 3(12):e222 SGD PMID 18069899
- Jump up ↑ Zewail A, et al. (2003) Novel functions of the phosphatidylinositol metabolic pathway discovered by a chemical genomics screen with wortmannin. Proc Natl Acad Sci U S A 100(6):3345-50 SGD PMID 12615994
See Help:Categories on how to add the wiki page for this gene to a Category </protect>