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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.
Gene Name: | myosin, light chain 3, alkali; ventricular, skeletal, slow |
Synonyms: | MYL3, CMH8, Cardiac myosin light chain 1, CMLC1, Myosin, light chain 3, alkali, Myosin light chain 3, Ventricular, skeletal, slow, VLC1, MLC1SB, MLC1V |
Target Sequences: | NM_000258 NP_000249.1 P08590 |
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