CYP26C1 Gene

cytochrome P450, family 26, subfamily C, polypeptide 1

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 enzyme is involved in the catabolism of all-trans- and 9-cis-retinoic acid, and thus contributes to the regulation of retinoic acid levels in cells and tissues. This gene is adjacent to a related gene on chromosome 10q23.33. [provided by RefSeq, Jul 2008]

cyp26c1 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term cyp26c1 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

CYP26C1 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for CYP26C1 from the Pathway Commons Protein-Protein Interactions dataset.

Defective CYP26C1 causes Focal facial dermal dysplasia 4 (FFDD4) Gene Set

From Reactome Pathways

proteins participating in the Defective CYP26C1 causes Focal facial dermal dysplasia 4 (FFDD4) pathway from the Reactome Pathways dataset.