Cytochrome P450, Family 7, Subfamily B, Member 1

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OMIM Number

603711

NCBI Gene ID

9420

Uniprot ID

O75881

Length

212,163 bases

No. of Exons

10

Protein Name

Cytochrome P450 7B1

Molecular Mass

58,256 Da

Amino Acid Count

506

Genomic Location

chr8:64,586,575-64,798,737

Gene Map Locus
8q12.3

Description

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. This endoplasmic reticulum membrane protein catalyzes the first reaction in the cholesterol catabolic pathway of extrahepatic tissues, which converts cholesterol to bile acids. This enzyme likely plays a minor role in total bile acid synthesis, but may also be involved in the development of atherosclerosis, neurosteroid metabolism and sex hormone synthesis. Mutations in this gene have been associated with hereditary spastic paraplegia (SPG5 or HSP), an autosomal recessive disorder. [From RefSeq]

Epidemiology in the Arab World

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Variant NameCountryGenomic LocationClinvar Clinical SignificanceCTGA Clinical Significance Condition(s)HGVS ExpressionsdbSNPClinvar
NM_004820.5:c.1057G>TSaudi ArabiaNC_000008.11:g.64615026C>ALikely PathogenicSpastic Paraplegia 5A, Autosomal Recessive; Bile Acid Synthesis Defect, Congenital, 3NG_008338.2:g.188766G>T; NM_004820.5:c.1057G>T; NP_004811.1:p.Glu353Ter
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