PDCD7 Polyclonal Antibody, 50ul Electrophoresis & Labeling Mutations in SMC1A result in

Mutations in SMC1A result in Cornelia de Lange syndrome

but on the opposite strand on chromosome 19

It is a signaling molecule that can interact with potassium channels and receptors| as well as other signaling molecules

The protein encoded by this gene belongs to the pancreatic ribonuclease family

is also located on chromosome 18

PDCD7 Polyclonal Antibody, 50ul Electrophoresis & Labeling Mutations in SMC1A result inThis gene encodes a 59 kDa protein that is associated with the U11 small nuclear ribonucleoprotein (snRNP), which is a component of the minor U12 type spliceosome responsible for catalyzing pre mRNA splicing of U12 type introns.