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Na+ CP type IX Alpha Polyclonal Antibody, 100ul Bottles Mutations in this gene have
Na+ CP type IX Alpha Polyclonal Antibody, 100ul Bottles Mutations in this gene have
Na+ CP type IX Alpha Polyclonal Antibody, 100ul Bottles Mutations in this gene have
Na+ CP type IX Alpha Polyclonal Antibody, 100ul Bottles Mutations in this gene have

Na+ CP type IX Alpha Polyclonal Antibody, 100ul Bottles Mutations in this gene have

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Na+ CP type IX Alpha Polyclonal Antibody, 100ul Bottles Mutations in this gene haveSCN9A encodes a voltage gated sodium channel which plays a significant role in nociception signaling. Mutations in SCN9A have been associated with primary erythermalgia, channelopathy associated insensitivity to pain, and paroxysmal extreme pain disorder.

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Description

Mutations in this gene have been associated with Coffin-Lowry syndrome (CLS)

Mutations in this gene have been found in individuals with autosomal dominant mental retardation

and adenocarcinoma of lung

The gene is located near the Smith-Magenis syndrome region on chromosome 17

Na+ CP type IX Alpha Polyclonal Antibody, 100ul Bottles Mutations in this gene haveSCN9A encodes a voltage gated sodium channel which plays a significant role in nociception signaling. Mutations in SCN9A have been associated with primary erythermalgia, channelopathy associated insensitivity to pain, and paroxysmal extreme pain disorder.

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