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PMR1 Monoclonal Antibody, 100ul Monoclonal Antibody Preparation Mutations in this gene are

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PMR1 Monoclonal Antibody, 100ul Monoclonal Antibody Preparation Mutations in this gene areThe protein encoded by this gene belongs to the family of P type cation transport ATPases. This magnesium dependent enzyme catalyzes the hydrolysis of ATP coupled with the transport of calcium ions. Defects in this gene cause Hailey Hailey disease, an autosomal dominant disorder. Alternatively spliced transcript variants encoding different isoforms have been identified.

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Description

Mutations in this gene are associated with microphthalmia

Rac GTPase activating protein 1 plays a regulatory role in cytokinesis

The protein encoded by MED26 (mediator complex subunit 26) is a subunit of the CRSP (cofactor required for SP1 activation) complex

NA polymerase that promotes microhomology-mediated end-joining (MMEJ)

PMR1 Monoclonal Antibody, 100ul Monoclonal Antibody Preparation Mutations in this gene areThe protein encoded by this gene belongs to the family of P type cation transport ATPases. This magnesium dependent enzyme catalyzes the hydrolysis of ATP coupled with the transport of calcium ions. Defects in this gene cause Hailey Hailey disease, an autosomal dominant disorder. Alternatively spliced transcript variants encoding different isoforms have been identified.

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