Difference between revisions of "YOR291W"

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|valign="top" nowrap bgcolor="{{SGDblue}}"| '''Coordinates'''
 
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|nowrap| Chr XV:861174..865592
 
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==Community Commentary==
 
==Community Commentary==
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==References==
 
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Revision as of 08:18, 30 January 2007

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Systematic name YOR291W
Gene name
Aliases
Feature type ORF, Uncharacterized
Coordinates Chr XV:861174..865592


Description of YOR291W: Hypothetical protein




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Community Commentary

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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]


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References

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  1. 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
  2. 2.0 2.1 submitted by Stephen R. Cronin on 2003-06-13

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