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MYL3

MYL3 encodes myosin light chain 3, an alkali light chain also referred to in the literature as both the ventricular isoform and the slow skeletal muscle isoform. Mutations in MYL3 have been identified as a cause of mid-left ventricular chamber type hypertrophic cardiomyopathy.
Protein class

Candidate cardiovascular disease genes, Disease related genes, Human disease related genes, Plasma proteins

Predicted location

Intracellular

Single cell type specificity

Cell type enriched (Cardiomyocytes)

Immune cell specificity

Not detected in immune cells

Cell line specificity

Cell line enhanced (CACO-2, HSkMC, RPTEC TERT1)

Interaction

Myosin is a hexamer of 2 heavy chains and 4 light chains.

Molecular function

Motor protein, Muscle protein, Myosin

More Types Infomation

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For Research Use Only. Not For Clinical Use.

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