CYP26B1 cytochrome P450 family 26 subfamily B member 1 [ Homo sapiens (human) ]
Source: NCBI Gene (ID 56603)
Symbol: CYP26B1
Full name: cytochrome P450 family 26 subfamily B member 1
Gene type: protein coding
RefSeq status: REVIEWED
Organism: Homo sapiens
Also known as: CYP26A2; P450RAI-2; P450RAI2; RHFCA
Summary: This gene encodes a member of the cytochrome P450 superfamily. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. The encoded protein is localized to the endoplasmic reticulum, and functions as a critical regulator of all-trans retinoic acid levels by the specific inactivation of all-trans retinoic acid to hydroxylated forms. Mutations in this gene are associated with radiohumeral fusions and other skeletal and craniofacial anomalies, and increased levels of the encoded protein are associated with atherosclerotic lesions. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2013]
Expression: Broad expression in testis (RPKM 9.5), skin (RPKM 9.2) and 21 other tissues
Orthologs: mouse
Gene size: 18625bp
Exon count: 9