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DHCR7

7-dehydrocholesterol reductase

DHCR7 is an enzyme that removes the C(7-8) double bond in the B ring of sterols and catalyzes the conversion of 7-dehydrocholesterol to cholesterol. This gene is ubiquitously expressed and its transmembrane protein localizes to the endoplasmic reticulum membrane and nuclear outer membrane. Mutations in this gene cause Smith-Lemli-Opitz syndrome (SLOS); a syndrome that is metabolically characterized by reduced serum cholesterol levels and elevated serum 7-dehydrocholesterol levels and phenotypically characterized by mental retardation, facial dysmorphism, syndactyly of second and third toes, and holoprosencephaly in severe cases to minimal physical abnormalities and near-normal intelligence in mild cases. Alternative splicing results in multiple transcript variants that encode the same protein.

Gene Name: 7-dehydrocholesterol reductase
Synonyms: DHCR7, 7-dehydrocholesterol reductase, 7-DHC reductase, D7SR, Delta7-sterol reductase, SLOS, Sterol delta-7-reductase, Putative sterol reductase SR-2, Smith-Lemli-Opitz syndrome, Sterol Delta(7)-reductase
Target Sequences: NM_001360 NP_001351.2 Q9UBM7

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For RESEARCH USE ONLY. Intended for use by laboratory professionals. Not intended for human diagnostic or therapeutic purposes.

The data on this page has been compiled from LifeSpan internal sources, the National Center for Biotechnology Information (NCBI), and The Universal Protein Resource (UniProt).