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]

PHYH Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for PHYH from the Pathway Commons Protein-Protein Interactions dataset.

PHYH Gene Set

From LINCS L1000 CMAP CRISPR Knockout Consensus Signatures

genes differentially expressed following the PHYH gene perturbation from the LINCS L1000 CMAP CRISPR Knockout Consensus Signatures dataset.

PHYH Gene Set

From CM4AI KOLF21J CRISPRi Gene Perturbation Atlas

genes differentially expressed following the PHYH gene perturbation from the CM4AI KOLF21J CRISPRi Gene Perturbation Atlas.