CYP26B1 Chromosome 2
Cytochrome P450 family 26 subfamily B member 1
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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
RS142156843
Conflicting classifications of pathogenicity
CYP26B1-related disorder, Inborn genetic diseases, CYP26B1-related disorder
Health Risk
RS143622603
Conflicting classifications of pathogenicity
CYP26B1-related disorder, CYP26B1-related disorder
Health Risk
RS146011965
Conflicting classifications of pathogenicity
Health Risk
RS61751056
Conflicting classifications of pathogenicity
Health Risk
RS76025186
Conflicting classifications of pathogenicity
CYP26B1-related disorder, CYP26B1-related disorder
Health Risk
RS1677161997
Likely pathogenic
Lethal occipital encephalocele-skeletal dysplasia syndrome, Lethal occipital encephalocele-skeletal dysplasia syndrome
Health Risk
RS281875231
Likely pathogenic
Lethal occipital encephalocele-skeletal dysplasia syndrome, Lethal occipital encephalocele-skeletal dysplasia syndrome
Health Risk
RS756077143
Likely pathogenic
Lethal occipital encephalocele-skeletal dysplasia syndrome, Lethal occipital encephalocele-skeletal dysplasia syndrome
Health Risk
RS281875232
Pathogenic
Lethal occipital encephalocele-skeletal dysplasia syndrome, Lethal occipital encephalocele-skeletal dysplasia syndrome
Health Risk
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 |