YOR291W
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| Systematic name | YOR291W | |
| Gene name | ||
| Aliases | ||
| Feature type | ORF, Uncharacterized | |
| Coordinates | Chr XV:861174..865592 | |
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Description of YOR291W: Hypothetical protein
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]
Contents
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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]
References
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- ↑ Jump up to: 1.0 1.1 1.2 1.3 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 2.2 2.3 submitted by Stephen R. Cronin on 2003-06-13
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