MYL3 wt Allele
**Semantic type:** Gene or Genome
**Definition:** Human MYL3 wild-type allele is located in the vicinity of 3p21.31 and is approximately 47 kb in length. This allele, which encodes myosin light chain 3 protein, is involved in binding to myosin heavy chains in sarcomeres. Mutations in the gene are associated with hypertrophic cardiomyopathy 8.
**Synonyms:** - CMH8 - ELC of Myosin Gene - Essential Light Chain of Myosin Gene - MLC-lV/sb - MLC1SB - MLC1V - Myosin Light Chain 3 wt Allele - Myosin, Light Chain 1, Slow, B Gene - Myosin, Light Chain 1, Ventricular Gene - Myosin, Light Chain 3, Alkali, Ventricular, Skeletal, Slow Gene - Myosin, Light Chain 3, Alkali; Ventricular, Skeletal, Slow Gene - Myosin, Light Polypeptide 3, Alkali; Ventricular, Skeletal, Slow Gene - VLC1 - VLCl
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Cross-system equivalences0
No cross-system equivalences mapped for this node.