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PHYH, phytanoyl-CoA 2-hydroxylase

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PHYH, phytanoyl-CoA 2-hydroxylase

  • 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]

  • Gene Synonyms (phytanoyl-CoA dioxygenase, peroxisomal, phytanic acid oxidase, phytanoil-CoA alpha hydroxylase, phytanoyl-CoA 2 oxoglutarate dioxygenase, phytanoyl-CoA alpha-hydroxylase, LN1, LNAP1, PAHX, PHYH1, RD,)
  • NCBI Gene ID: 5264
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>O14832
  • View the NCBI Database for this Gene »

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

phytanoyl-CoA 2-hydroxylase interacts with:

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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