Name

PHYH Gene

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]

PHYHIP Gene

phytanoyl-CoA 2-hydroxylase interacting protein

Enables protein tyrosine kinase binding activity. Involved in protein localization. Located in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025]

PHYHD1 Gene

phytanoyl-CoA dioxygenase domain containing 1

Enables 2-oxoglutarate-dependent dioxygenase activity. [provided by Alliance of Genome Resources, Mar 2025]

PHYHIPL Gene

phytanoyl-CoA 2-hydroxylase interacting protein-like

Located in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025]

Phytanoyl-CoA Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the Phytanoyl-CoA metabolite from the curated HMDB Metabolites of Enzymes dataset.