YOR291W
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| Systematic name | YOR291W |
| Gene name | YPK9 |
| Aliases | |
| Feature type | ORF, Verified |
| Coordinates | Chr XV:861174..865592 |
| Primary SGDID | S000005817 |
Description of YOR291W: Vacuolar protein of unknown function; shares sequence similarity with the type V P-type ATPase Spf1p; null mutant is hypersensitive to manganese; homolog of human ATP13A2 (PARK9), mutations in which are associated with Parkinson disease 9[1][2][3]
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Contents
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. [4] [5]
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. [4] [5]
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References
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- ↑ Gitler AD, et al. (2009) Alpha-synuclein is part of a diverse and highly conserved interaction network that includes PARK9 and manganese toxicity. Nat Genet 41(3):308-15 SGD PMID 19182805
- ↑ Catty P, et al. (1997) The complete inventory of the yeast Saccharomyces cerevisiae P-type transport ATPases. FEBS Lett 409(3):325-32 SGD PMID 9224683
- ↑ Cronin SR, et al. (2002) Cod1p/Spf1p is a P-type ATPase involved in ER function and Ca2+ homeostasis. J Cell Biol 157(6):1017-28 SGD PMID 12058017
- ↑ 4.0 4.1 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
- ↑ 5.0 5.1 submitted by Stephen R. Cronin on 2003-06-13
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