CYP27B1 cytochrome P450 family 27 subfamily B member 1 [ Homo sapiens (human) ]
Source: NCBI Gene (ID 1594)
Source: NCBI Gene (ID 1594)
Symbol: CYP27B1
Full name: cytochrome P450 family 27 subfamily B member 1
Gene type: protein coding
RefSeq status: REVIEWED
Organism: Homo sapiens
Also known as: CP2B; CYP1; CYP1alpha; CYP27B; P450c1; PDDR; VDD1; VDDR; VDDRI; VDR
Summary: 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. The protein encoded by this gene localizes to the inner mitochondrial membrane where it hydroxylates 25-hydroxyvitamin D3 at the 1alpha position. This reaction synthesizes 1alpha,25-dihydroxyvitamin D3, the active form of vitamin D3, which binds to the vitamin D receptor and regulates calcium metabolism. Thus this enzyme regulates the level of biologically active vitamin D and plays an important role in calcium homeostasis. Mutations in this gene can result in vitamin D-dependent rickets type I. [provided by RefSeq, Jul 2008]
Expression: Biased expression in kidney (RPKM 9.5), thyroid (RPKM 4.8) and 4 other tissues
Orthologs: mouse
Gene size: 4745bp
Exon count: 9