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MYL2, myosin light chain 2

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MYL2, myosin light chain 2

  • Thus gene encodes the regulatory light chain associated with cardiac myosin beta (or slow) heavy chain. Ca+ triggers the phosphorylation of regulatory light chain that in turn triggers contraction. Mutations in this gene are associated with mid-left ventricular chamber type hypertrophic cardiomyopathy. [provided by RefSeq, Jul 2008]

  • Gene Synonyms (CMH10, MLC-2s/v, MLC2, myosin regulatory light chain 2, ventricular/cardiac muscle isoform, MLC-2, MLC-2v, RLC of myosin, cardiac myosin light chain 2, cardiac ventricular myosin light chain 2, myosin light chain 2, slow skeletal/ventricular muscle isoform, myosin, light chain 2, regulatory, cardiac, slow, myosin, light polypeptide 2, regulatory, cardiac, slow, regulatory light chain of myosin, slow cardiac myosin regulatory light chain 2, ventricular myosin light chain 2,)
  • NCBI Gene ID: 4633
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>P10916
    UNIPROT ID#>>Q6IB42
  • View the NCBI Database for this Gene »

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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