Reaction: Defective CYP2R1 does not 25-hydroxylate vitamin D
- in pathway: Defective CYP27B1 causes VDDR1B
The first step in vitamin D3 activation requires 25-hydroxylation of vitamin D3 (or vitamin D2), mediated by vitamin D 25-hydroxylase (CYP2R1). Defects in CYP2R1 can cause rickets, vitamin D-dependent 1B (VDDR1B; MIM:600081), a disorder caused by a selective deficiency of the active form of vitamin D (CTL) resulting in defective bone mineralization and clinical features of rickets. The missense mutation L99P can cause VDDR1B (Cheng et al. 2004, Casella et al. 2004). When plasma levels of 25-hydroxyvitamin D3 (calcidiol, CDL) are low, classic symptoms of vitamin D deficiency, including skeletal abnormalities, hypocalcemia, and hypophosphatemia, are observed.
Reaction - small molecule participants:
H+ [cytosol]
O2 [cytosol]
VD3 [endoplasmic reticulum membrane]
NADPH [cytosol]
Reactome.org reaction link: R-HSA-5602147
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Reaction input - small molecules:
hydron
dioxygen
calciol
NADPH(4-)
Reaction output - small molecules:
Reactome.org link: R-HSA-5602147