Aliases for CYP4F22 Gene
External Ids for CYP4F22 Gene
Previous GeneCards Identifiers for CYP4F22 Gene
This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This gene is part of a cluster of cytochrome P450 genes on chromosome 19 and encodes an enzyme thought to play a role in the 12(R)-lipoxygenase pathway. Mutations in this gene are the cause of ichthyosis lamellar type 3. [provided by RefSeq, Jul 2008]
GeneCards Summary for CYP4F22 Gene
CYP4F22 (Cytochrome P450 Family 4 Subfamily F Member 22) is a Protein Coding gene. Diseases associated with CYP4F22 include Ichthyosis, Congenital, Autosomal Recessive 5 and Congenital Ichthyosiform Erythroderma. Among its related pathways are Arachidonic acid metabolism and Metabolism. Gene Ontology (GO) annotations related to this gene include iron ion binding and oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen. An important paralog of this gene is CYP4F2.