CYP26B1 Chromosome 2

Cytochrome P450 family 26 subfamily B member 1
9 variants 9 Health Risk

Upload your DNA to see your personal genotypes for variants in CYP26B1.

What This Gene Does
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]
Gene Info
Gene Group
Cytochrome P450 family 26
Locus Type
gene with protein product
Location
2p13.2
Ensembl
ENSG00000003137
Associated Conditions (3)
CYP26B1-related disorder
Inborn genetic diseases
Lethal occipital encephalocele-skeletal dysplasia syndrome
Key Variants
All Variants (9)
RSID Category Clinical Significance Conditions
RS142156843 Health Risk Conflicting classifications of pathogenicity CYP26B1-related disorder, Inborn genetic diseases, CYP26B1-related disorder
RS143622603 Health Risk Conflicting classifications of pathogenicity CYP26B1-related disorder, CYP26B1-related disorder
RS146011965 Health Risk Conflicting classifications of pathogenicity
RS61751056 Health Risk Conflicting classifications of pathogenicity
RS76025186 Health Risk Conflicting classifications of pathogenicity CYP26B1-related disorder, CYP26B1-related disorder
RS1677161997 Health Risk Likely pathogenic Lethal occipital encephalocele-skeletal dysplasia syndrome, Lethal occipital encephalocele-skeletal dysplasia syndrome
RS281875231 Health Risk Likely pathogenic Lethal occipital encephalocele-skeletal dysplasia syndrome, Lethal occipital encephalocele-skeletal dysplasia syndrome
RS756077143 Health Risk Likely pathogenic Lethal occipital encephalocele-skeletal dysplasia syndrome, Lethal occipital encephalocele-skeletal dysplasia syndrome
RS281875232 Health Risk Pathogenic Lethal occipital encephalocele-skeletal dysplasia syndrome, Lethal occipital encephalocele-skeletal dysplasia syndrome
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