Gamma Tubulin mouse Monoclonal Antibody(6C12), 100ul Proteases Mutations in this gene have

Mutations in this gene have been associated with thyroid dysgenesis

a rare immunodeficiency characterized by extreme susceptibility to infection with Epstein-Barr virus

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Diseases associated with HSPA14 include tetralogy of fallot

and the rest are the products of nuclear genes

Gamma Tubulin mouse Monoclonal Antibody(6C12), 100ul Proteases Mutations in this gene haveThis gene encodes a member of the tubulin superfamily. The encoded protein localizes to the centrosome where it binds to microtubules as part of a complex referred to as the gamma tubulin ring complex. The protein mediates microtubule nucleation and is required for microtubule formation and progression of the cell cycle. A pseudogene of this gene is found on chromosome 7.