DHCR7 Break Apart FISH Probe

This gene encodes 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 cognitive disability, 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.[provided by RefSeq, Aug 2009]


Gene Details
SKU Test Kits Buffer Dye Color Order Now
DHCR7BA-20-REGO 20 (40 μL) 200 μL color color Request Pricing
DHCR7BA-20-REGR 20 (40 μL) 200 μL color color Request Pricing
DHCR7BA-20-ORGR 20 (40 μL) 200 μL color color Request Pricing
DHCR7BA-20-GOGR 20 (40 μL) 200 μL color color Request Pricing
DHCR7BA-20-GRRE 20 (40 μL) 200 μL color color Request Pricing
DHCR7BA-20-GROR 20 (40 μL) 200 μL color color Request Pricing
DHCR7BA-20-GRGO 20 (40 μL) 200 μL color color Request Pricing
DHCR7BA-20-AQOR 20 (40 μL) 200 μL color color Request Pricing

Gene Summary

This gene encodes 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 cognitive disability, 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.[provided by RefSeq, Aug 2009]

Gene Details

Gene Symbol : DHCR7

Gene Name : 7-dehydrocholesterol reductase

Chromosome : CHR 11: 714,484,30-714,344,10

Locus : 11q13.4

Alt. Genes : OPTN

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