PHYH 抗体
(Phytanoyl-CoA 2-Hydroxylase (PHYH))
This gene is a member of the PhyH family and encodes a peroxisomal protein that is involved in the alpha-oxidation of 3-methyl branched fatty acids. Specifically, this protein converts phytanoyl-CoA to 2-hydroxyphytanoyl-CoA. Mutations in this gene have been associated with Refsum disease (RD) and deficient protein activity has been associated with Zellweger syndrome and rhizomelic chondrodysplasia punctata. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008].
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Latest Publications for our PHYH 抗体
: "Recovery of PEX1-Gly843Asp peroxisome dysfunction by small-molecule compounds." in: Proceedings of the National Academy of Sciences of the United States of America, Vol. 107, Issue 12, pp. 5569-74, (2010) (PubMed).: "Large-scale mapping of human protein-protein interactions by mass spectrometry. ..." in: Molecular systems biology, Vol. 3, pp. 89, (2007) (PubMed).
Aliases for PHYH 抗体
phytanoyl-CoA 2-hydroxylase (PHYH) 抗体phytanoyl-CoA hydroxylase-like (LOC478001) 抗体
phytanoyl-CoA 2-hydroxylase (phyh) 抗体
phytanoyl-CoA 2-hydroxylase (Phyh) 抗体
phytanoyl-CoA hydroxylase (Phyh) 抗体
AI256161 抗体
AI265699 抗体
LN1 抗体
LNAP1 抗体
Lnap1 抗体
PAHX 抗体
PHYH1 抗体
RD 抗体
zgc:110203 抗体
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