MYOZ2 (Myozenin 2) is a Protein Coding gene. Diseases associated with MYOZ2 include Cardiomyopathy, Hypertrophic, 16 and Myoz2-Related Familial Hypertrophic Cardiomyopathy. GO annotations related to this gene include actin binding and telethonin binding. An important paralog of this gene is MYOZ1.The protein encoded by this gene belongs to a family of sarcomeric proteins that bind to calcineurin, a phosphatase involved in calcium-dependent signal transduction in diverse cell types. These family members tether calcineurin to alpha-actinin at the z-line of the sarcomere of cardiac and skeletal muscle cells, and thus they are important for calcineurin signaling. Mutations in this gene cause cardiomyopathy familial hypertrophic type 16, a hereditary heart disorder.
A synthesized peptide derived from human Myozenin2, corresponding to a region within the internal amino acids.
A synthesized peptide derived from human MYPOP.
A synthesized peptide derived from human MYPT1, corresponding to a region within C-terminal amino acids.
A synthesized peptide derived from human MYPT1.
A synthesized peptide derived from human MYPT1, corresponding to a region within the internal amino acids.
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