| Name |
|---|
PHYH Genephytanoyl-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 Genephytanoyl-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 Genephytanoyl-CoA dioxygenase domain containing 1 Enables 2-oxoglutarate-dependent dioxygenase activity. [provided by Alliance of Genome Resources, Mar 2025] |
PHYHIPL Genephytanoyl-CoA 2-hydroxylase interacting protein-like Located in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
Phytanoyl-CoA Gene SetFrom HMDB Metabolites of Enzymes interacting proteins for the Phytanoyl-CoA metabolite from the curated HMDB Metabolites of Enzymes dataset. |